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Author Archive

Tumors in animals

Monday, July 4th, 2005

My youngest brother has been reading “healthy eating” books, and was telling me that wild animals don’t get cancer. He wasn’t content with my correction and wanted some evidence. Fair enough. Looking around online, I found a few references and was reminded of the Laetrile nonsense.

Laetrile was a quack cancer cure popular in the 70’s. The tout was that sharks don’t get cancer, and that taking pills made from ground up shark cartilage would cure cancer. This paragraph give a summary of the Laetrile cure fad:

Crude shark cartilage extract is not a cure for cancer in humans
Promotion of cartilage extracts from sharks has had two negative outcomes: a decline in shark populations, and a diversion of patients from effective cancer treatment. The argument has been that sharks don’t get cancer. However, both malignant and benign neoplasms of sharks and their relatives were described by Gary Ostrander and associates at Johns Hopkins University (Maryland), Penn State College of Medicine, and Registry of Tumors in Lower Animals (Virginia). So far there is no evidence to support the use of crude cartilage nor any cartilage extract to reach and eradicate cancer cells. The authors see the use of shark cartilage extracts as another example of pseudoscience used in decision making where the facts are not considered. (Cancer Research 64: 8485-8491, 2004)

The reference to the Registry of Tumors in Lower Animals sounds intriguing so I looked it up. The collection is searchable online after registering, and I’ve included a link. The Registry includes many cases of cancer in wild animals.

Looking around a bit more, I find someone else has considerately done a search of the literature, and posted abstracts. I’ve includes them below (lost track of the original source). These reports come from journals indexed by Pubmed which indexes biomedical journals, so papers in ecological or field biology journals would be missed. As you can see, there are many reports describing cancer in wild animals. The list is long, but skimming shows that tumors in wild animals have been observed many times.

Next up, I’ll look into the notion you’ve gotten that microwaving your food makes it dangerous to eat.

Cesk Patol 1996 May;32(2):78-83

[Tumors in wildlife].

[Article in Czech]

Karpenko A, Bukovjan K.

Oddeleni patologie SZZ, Benesov u Prahy.

Wild animal tumours have not been much studied yet. Authors found six
mostly benign cases in Czech Republic in checking hunts between the years
1988 and 1993: Mature differentiated ovarian teratoma and apocrine skin
adenoma in field hare, intraductal mammary papillomatosis in a roe,
complex odontoma and pleomorphic mammary carcinoma (single malignancy in
the group) in fox. A soft tissue tumour in a fallow-buck’s neck could not
be histogenetically classified. A high structural equivalence of animal
and human tumours allows using ICD-O classification as a whole.

PMID: 9560906 [PubMed – indexed for MEDLINE]

J Vet Med Sci 1997 Aug;59(8):703-6

Spontaneous gastric carcinoid tumors in the striped field mouse (Apodemus
agrarius).

Oh SW, Chae C, Jang D.

Department of Veterinary Pathology, College of Veterinary Medicine, Seoul
National University, Suwon, Kyounggi-Do, Republic of Korea.

Gastric carcinoid tumors were found in seven of 135 striped field mice
(Apodemus agrarius) by routine histopathologic examination. All these
carcinoids occurred in mature striped field mice aged 72-100 weeks. Six
animals were females and only one was male. Only two of seven tumors were
detectable by gross examination. Grossly, tumors were located in the
fundus of the glandular stomach. All seven tumors were microscopically
single in the stomach and two mice exhibited extragastric metastasis.
Tumors from all the mice were characterized by densely packed sheets of
round to polygonal cells, subdivided into packets by a fine fibrovascular
stroma. The cytoplasm of all tumor cells from all the mice contained
argyrophil granules when stained by Grimelius and Sevier-Munger silver
procedures. All seven mice with gastric carcinoids exhibited positive
immunoreactivity to neuron specific enolase. Psammoma bodies,
concentrically laminated microcalcification, were characteristic findings
in gastric carcinoids from five mice. There were also a concomitant and
independent hepatocellular adenoma in one case and hepatocellular
carcinoma in two cases. The present cases provide the first description
of spontaneous gastric carcinoid tumors in the striped field mice.

PMID: 9300368 [PubMed – indexed for MEDLINE]

Leukemia 1997 Apr;11 Suppl 3:170-1

Plasmacytoid leukemia of chinook salmon.

Kent ML, Eaton WD, Casey JW.

Department of Fisheries and Oceans, Pacific Biological Station, Nanaimo,
B.C., Canada.

Plasmacytoid leukemia is a common disease of seawater pen-reared chinook
salmon (Oncorhynchus tshawytscha) in British Columbia, Canada, but has
also been detected in wild salmon, in freshwater-reared salmon in United
States, and in salmon from netpens in Chile. The disease can be
transmitted under laboratory conditions, and is associated with a
retrovirus, the salmon leukemia virus. However, the proliferating
plasmablasts are often infected with the microsporean Enterocytozoon
salmonis, which may be an important co-factor in the disease.

PMID: 9209333 [PubMed – indexed for MEDLINE]

Pathol Int 1996 Dec;46(12):919-32

Mouse mammary tumor virus and mammary tumorigenesis in wild mice.

Imai S.

Nara Prefectural Institute of Public Health, Japan.

The current knowledge of the distribution of the mouse mammary tumor
virus (MMTV) proviral genomes and the mechanism of mammary tumorigenesis
by MMTV in mice, with the main emphasis on Asian feral mice, is reviewed.
The relevant earlier discoveries on the mode of MMTV transmission are
summarized to provide an outline of the biology of MMTV. Finally, the
viral etiology of human breast cancer will be discussed.

Publication Types:
Review
Review, academic

PMID: 9110343 [PubMed – indexed for MEDLINE]

Adv Neurol 1991;56:473-9

Retroviral leukemia and lower motor neuron disease in wild mice: natural
history, pathogenesis, and genetic resistance.

Gardner MB.

Department of Pathology, School of Medicine, University of California, Davis
95616.

Publication Types:
Review
Review, tutorial

PMID: 1649545 [PubMed – indexed for MEDLINE]

J Wildl Dis 1985 Oct;21(4):386-90

Diseases diagnosed in wild turkeys (Meleagris gallopavo) of the southeastern
United States.

Davidson WR, Nettles VF, Couvillion CE, Howerth EW.

Diagnostic findings are presented on 139 sick or dead wild turkeys
examined during the period 1972 through 1984. Turkeys originated from
eight southeastern states (Alabama, Arkansas, Florida, Georgia, South
Carolina, Tennessee, Virginia, West Virginia) and included 31 turkeys
categorized as capture-related mortalities and 108 turkeys categorized as
natural mortalities. Frequent diagnoses (greater than or equal to 10% of
case accessions) in the natural mortality group were trauma, avian pox,
and histomoniasis. Less frequent diagnoses (less than or equal to 4% of
case accessions) included malnutrition/environmental stress syndrome,
coligranuloma-like condition, crop impaction, bumblefoot, organophosphate
toxicosis, infectious sinusitis, a lympho-proliferative disease,
salmonellosis, aspergillosis, toxoplasmosis, crop trichomoniasis, and
melorheostosis.

PMID: 4078973 [PubMed – indexed for MEDLINE]

Acta Vet Scand 1985;26(1):61-71

Leukaemic neoplasia in free-living mammals in Denmark.

Elvestad K, Henriques UV.

PMID: 3839967 [PubMed – indexed for MEDLINE]

Int J Cancer 1981 Aug 15;28(2):241-7

Natural killer cell activity in a population of leukemia-prone wild mice
(Mus musculus).

Scott JL, Pal BK, Rasheed S, Gardner MB.

Natural cell-mediated cytotoxicity against YAC-I targets was measured in
splenocytes from leukemia-prone wild mice trapped near Lake Casitas (LC)
in southern California. Cytotoxicity was mediated by cells that were
non-adherent to nylon wool, non-phagocytic and resistant to thy-1.2
antiserum plus complement. Natural MuLV viremia in LC mice did not impair
splenic cytotoxicity against TAC-I target cells, Cells infected with
amphotropic and ecotropic MuLV of wild mouse origin were not appreciably
lysed by LC splenic effectors. Although variable levels of cytotoxicity
were detected against TAC-1 by normal spleen cells, consistently low
levels of cytotoxicity against allogenic LC lymphoma, sarcoma and
carcinoma targets were found using the same splenocytes. These results
indicate that LC mice possess splenocytes with the characteristics of
natural killer (NK) cells as defined in inbred mice. The resistance of
LC-derived targets to lysis by LC NK cells suggests that NK cells may not
be involved in natural tumor immunosurveillance or that the development
of spontaneous tumors may involve escape from NK-mediated effector
mechanisms.

PMID: 6274813 [PubMed – indexed for MEDLINE]

Vet Pathol 1977 Nov;14(6):539-46

Gynecologic pathology in the rhesus monkey (Macaca mulatta). II. Findings in
laboratory and free-ranging monkeys.

DiGiacomo RF.

The most prevalent findings in reproductive tracts of 38 laboratory and
17 free-ranging Rhesus female monkeys were vaginitis, cervicitis,
metritis, pelvic endometriosis and uterine adenomyosis. Several monkeys
had cervical dysplasia and one had a serous cystadenoma. The findings in
the two groups were similar although prevalence for several diseases
differed. There was a significant relationship between the occurrence of
vaginitis, metritis, adenomyosis and endometriosis and gravidity, time
since last pregnancy, number of matings, hysterotomies, reproductive
ability and reproductive status.

PMID: 412291 [PubMed – indexed for MEDLINE]

J Wildl Dis 1999 Oct;35(4):804-7

Relating tumor score to hematology in green turtles with
fibropapillomatosis in Hawaii.

Work TM, Balazs GH.

U.S. Geological Survey, Biological Resource Division, National Wildlife
Health Center, Honolulu Field Station, Hawaii 96850, USA.
thierry_work@usgs.gov

The relationship between hematologic status and severity of tumor
affliction in green turtles (Chelonia mydas) with fibropapillomatosis
(FP) was examined. During 1 wk periods in July 1997 and July 1998, we
bled 108 free-ranging green turtles from Pala’au (Molokai, Hawaii, USA)
where FP is endemic. Blood was analyzed for hematocrit, estimated total
solids, total white blood cell (WBC) count and differential WBC count.
Each turtle was assigned a subjective tumor score ranging from 0 (no
visible external tumors) to 3 (heavily tumored) that indicated the
severity of FP. There was a progressive increase in monocytes and a
decrease in all other hematologic parameters except heterophils and total
numbers of white blood cells as tumor score increased. These data
indicate that tumor score can relate to physiologic status of green
turtles afflicted with FP, and that tumor score is a useful field monitor
of severity of FP in this species.

PMID: 10574546 [PubMed – indexed for MEDLINE]

J Wildl Dis 1999 Oct;35(4):753-62

Descriptive epidemiology of roe deer mortality in Sweden.

Aguirre AA, Brojer C, Morner T.

Department of Wildlife, The National Veterinary Institute, Uppsala, Sweden.
aguirre@wpti.org

A retrospective epidemiologic study was conducted to examine causes of
mortality of 985 wild roe deer (Capreolus capreolus) submitted to the
National Veterinary Institute (SVA; Uppsala, Sweden) from January 1986 to
December 1995. Age, sex, body condition, and geographic distribution as
related to disease conditions are reported herein. The most common causes
of mortality in roe deer were trauma (19%), winter starvation (18%),
gastritis/enteritis (15%), bacterial infections (11%), parasitic
infection (11%), systemic diseases (11%), neoplasia (2%), congenital
disorders (1%), and miscellaneous causes (6%). Cause of death was not
determined in 6% of the cases. The distribution of causes of death
reported in this study differ from previous works in Sweden in that
infectious and parasitic diseases were more common than winter
starvation. The pathologic findings in studies like this do not
necessarily represent what is occurring in the natural environment, but
they do provide a good indication of distribution of diseases over time
as well as age and sex structure in relation to disease conditions.
Further research and more detailed studies are in progress to better
understand specific mortality factors as well as etiologies of certain
described diseases in roe deer in Sweden.

PMID: 10574535 [PubMed – indexed for MEDLINE]

J Zoo Wildl Med 1999 Mar;30(1):165-9

Herpesvirus-associated papillomas in koi carp (Cyprinus carpio).

Calle PP, McNamara T, Kress Y.

Wildlife Health Sciences, Wildlife Conservation Society, Bronx, New York
10460-1099, USA.

From January through November 1994, 32% (7/22) of koi carp (Cyprinus
carpio) maintained in indoor aquariums developed proliferative cutaneous
lesions that consisted of single to multiple 2-10-mm whitish to pink
fleshy masses usually associated with fin rays. Although scaleless koi
were more commonly affected (3/6) than were normally scaled koi (4/16),
the difference in incidence rates was not significant (chi2 text, P >
0.05). Lesions typically resolved spontaneously in 1-3 wk, occasionally
persisted for >3 mo, and recurred in several fish after 2-5 mo. Fish were
otherwise asymptomatic. Wet mount preparations from lesions were densely
cellular and consisted of hyperplastic epidermal cells of normal
morphology without parasites or inflammatory cells. Histologically,
biopsies were consistent with papillomas and were characterized by a
marked benign epidermal hyperplasia without inclusion bodies or
inflammatory infiltrate. Transmission electron microscopic examination
revealed intranuclear and intracytoplasmic herpesvirus virions. Virus
isolation attempts were unsuccessful.

PMID: 10367660 [PubMed – indexed for MEDLINE]

J Wildl Dis 1999 Apr;35(2):392-4

Adenocarcinoma of the mammary gland in a red fox from Austria.

Janovsky M, Steineck T.

Research Institute of Wildlife Ecology, University of Veterinary Medicine,
Vienna, Austria.

A mammary gland adenocarcinoma was diagnosed in an adult red fox (Vulpes
vulpes) which was shot in Austria in August 1995. Metastases were found
in the kidneys and liver. This is the first reported case of an
adenocarcinoma in a fox, and lack of mammary gland carcinoma in this
species may be age related.

PMID: 10231770 [PubMed – indexed for MEDLINE]

Install new hard drives with Software RAID 1

Thursday, June 16th, 2005

This turned out to be pretty straightforward once I got the order of steps right. Don’t make the filesystems before the mkraid, you will end up with “bad superblock” errors later.

I added two 400Gb SATA hard drives in RAID1 to an existing system. I already had one pair of drives in RAID 1, the new drives form a new RAID array.

1) Phyiscally add the drives.

2) Run fdisk, make one partition on each drive.
fdisk /dev/hdc
fdisk /dev/hdd

3) Edit /etc/raidtab, add section for /dev/md1:
raiddev /dev/md1
raid-level 1
nr-raid-disks 2
chunk-size 256
persistent-superblock 1
nr-spare-disks 0
device /dev/sdc1
raid-disk 0
device /dev/sdd1
raid-disk 1

4) Make RAID, needed ‘force’ flag:
mkraid -f /dev/md1
mkraid -R /dev/md1

5) Make filesystems:
mke2fs -j /dev/sdc1
mke2fs -j /dev/sdd1

This takes 10 min or so.

6) Add new filesystem to /etc/fstab for automounting:
/dev/md1 /home ext3 defaults 1 2

And now the keychain drive gets pushed from sdc to sde:
/udev/sde1 /mnt/key vfat owner,kudzu 0 0

7) Mount new RAID:
mkdir /data
mount /data

Useful RAID commands:
more /proc/mdstat
mdadm -D /dev/md1

Useful guide:
Software-RAID-HOWTO

Graphviz on OS X

Sunday, May 8th, 2005

tried running the Graphviz programs on OS X (sudo fink install graphviz) and got a font error message, ‘Could not find/open font : Times in…’

To use the Graphviz programs with OS X, need to specify

-Nfontname=luxisr

The program can use fonts in /usr/X11R6/lib/X11/fonts/TTF. This is part of
the Apple supplied X11 (part of the optional/developer OS install disk? I don’t recall when/how I installed it.).
Found this info at: link

Nanobacteria, an estimate

Thursday, April 21st, 2005

I heard an assertion nanobacteria exist along with some speculation about them and so on. It was news to me and got me wondering if I had missed a discovery announcement, so I ran some numbers:

Consider a large nanobacteria, 30 nm by 100 nm. It has an approximate volume of 7e-23 m3.

How much DNA could this volume contain? Pop up a DNA molecule in Chime and get an estimate of dimensions: 20 bp run for 6.4 nm, so 0.32 nm / bp. The double helix has a radius of 1.3 nm.

Length of DNA with a volume equal to the cell = 7e-23 m3 / [ (1.3 nm)2 x π ] = 1.3e-5 m
Bps = length / bp length = 1.3e-5 m / 0.32 nm = 42 kb of DNA.

A low average bacterial gene length is 300 bp, so a nanobacteria could hold a maximum of 42 kb / 300 bp = 139 genes. The minimum number of genes for an independent living organism is 300 – 500, so a nanobacteria can’t have enough genes. It can’t exist. But let’s run the other numbers, on proteins.

A typical protein is 3 nm, lets call it a cube with a volume of (3 nm)3 = 2.7e-26m3.
A nanobacteria can hold 7e-23m3 / 2.7e-26m3 = 2600 proteins total. Low but not a hard limit on existence.

Now let’s put this together and describe a nanobacteria. 30% of the volume is water and small molecules. Of the remainder, let’s say 2/3 is DNA and 1/3 is protein. The nanobacteria contains enough DNA for 65 genes, and 600 proteins. Which means nanobacteria can’t exist, they are too small. There are quite a few unlikely bits in biology (pretty much every rule in biology has exceptions), so I’ll qualify it and say it is quite unlikely that nanobacteria exist. And to my estimates, add the evidence from projects to mass sequence DNA extracted from the environmental samples–if nanobacteria exist, their DNA would turn up in these projects, and no new phylum of sequences has emerged.

An E. coli by contrast is 1 µ x 3 µ and can hold 600 Mb of DNA and 20 million proteins. It’s genome is actually 4.6 Mb, and the extra space is taken up by a cell wall and protein.

Kernel upgrade

Thursday, April 21st, 2005

Upgraded the kernel on my linux server and it was the easiest thing ever:

yum upgrade kernel-smp

It updated grub and everything! Color me surprised. Linux is getting *so* easy to use.

Crafty octopus

Thursday, March 24th, 2005

Have a look at this octopus. It camoflages itself while it walks around.

Two tiny species of tropical octopus have demonstrated a remarkable disappearing trick. They adopt a two-armed ‘walk’ that frees up their remaining six limbs to camouflage them as they slink away from trouble.

View movies below the fold.
(more…)

Worst case sea level rise

Saturday, March 19th, 2005

From an interview with National Center for Atmospheric Research in Colorado’s Gerald Meehl discussing an NCAR paper in Science:

Experts say sea levels have risen 4 inches already over the past century and could rise between 4 and 40 inches more in the next century.

If completely melted, the Greenland ice sheet would add 25 feet to overall sea level and the West Antarctic Ice Sheet would raise it by 16 feet — enough to swamp most of Florida, Bangladesh and New York City’s Manhattan island.

So that’s the upper limit on sea level rise. And while the modelers predict a mm/year rate, ice sheets melt catastrophically and we’re getting into the range of losing some of them, so I’ll make a wild-ass guess that we’ll see a bad decade with a foot or so sea level rise this century.

(To digress, this reminds me of how bad the premise of Waterworld is. You know a movie’s science is bad when it makes you look fondly on the scientific plausibility of Planet of the Apes. Waterworld is a full point higher on the Scientfic Implausibility Richter scale.)

From the abstract of the paper, “The Climate Change Commitment”. Wigley, TML. (2005) Science 307:1766-9:

These constant-composition (CC) commitments and their uncertainties are quantified. Constant-emissions (CE) commitments are also considered. The CC warming commitment could exceed 1°C. The CE warming commitment is 2° to 6°C by the year 2400. For sea level rise, the CC commitment is 10 centimeters per century (extreme range approximately 1 to 30 centimeters per century) and the CE commitment is 25 centimeters per century (7 to 50 centimeters per century).

The CE senario predicts 2.5 mm/year rise, but emissions are rising so this is definitely an underestimate.

Bioinformatics books

Friday, March 18th, 2005

Notes on some bioinformatics books from two perspectives. Here’s what I’m looking for: 1) advanced discussion of computational and statistical methods for genomics, especially microarray analysis, and 2) suitability for an intro and survey bioinformatics course I teach.

THE ANALYSIS OF GENE EXPRESSION DATA: METHODS AND SOFTWARE
edited by Giovanni Parmigiani, Elizabeth S Garrett, Rafael A Irizarry, Scott L Zeger
companion website
Great medium depth howto. Covers R, dChip, SAM, and packages that take more sophisticated approaches to analysis, clustering, and visualization.

Bioinformatics for Geneticists
Edited by Michael R. Barnes and Ian C. Gray
Published Online: 22 May 2003
Genomic orientation, but too light and introductory for my needs, too genomic focused for my course. Good starting point book for a geneticist.

Advances in Systems Biology
Series: Advances in Experimental Medicine and Biology, Vol. 547
Opresko, Lee K.; Gephart, Julie M.; Mann, Michaela B. (Eds.)
2004
Pulled this book for A Systems Approach to Discovering Signaling and Regulatory Pathways—or how to digest large interaction networks into relevant pieces by Trey Ideker.

Microarray Gene Expression Data Analysis: A Beginners Guide
by Helen C. Causton , John Quackenbush , Alvis Brazma
2003
What it says it is: design, image processing, normalization, basic stats, clustering.

Bioinformatics: Databases and Systems
Edited by Stan Letovsky
Kluwer Academic Press, Boston, 1999
A chapter a database. Covers the usual gang, plus chapters on WIT/WIT2, KEGG, BioWidgets (Java), and AceDB (overview).

Statistical Methods in Bioinformatics An Introduction
Series: Statistics for Biology and Health
Ewens, Warren J. and Grant, Gregory
2nd ed. , 2004, 588p
errata
Heavy statistical treatment of sequence analysis. Starts with stats, then stat properties of one seq, multiple seq alignments, BLAST, Marlov chains, HMMs.

‘In Silico’ Simulation of Biological Processes
No. 247 Novartis Foundation Symposium
270 pages January 2003
Picked this up for the GO chapter. Also has a chapter on KEGG.

Micr
oarrays Methods and Applications: Nuts and Bolts

Edited by Gary Hardiman
2003
Covers topics from basic MA howtos to more specialized applications. A mixed bag. One chapter on microarray scanner evaluation, another on C. elegans 50-mer oligos made by the Hardiman lab at UCSD. Chapter text and figures are online.


Microarray Quality Control

by Wei Zhang, Ilya Shmulevich and Jaakko Astola
136 pages February 2004
What the title says. Microarrays from a core facility perspective. Ends with normatization. Covers long oligo design.

Microarray Bioinformatics
by Dov Stekel
Cambridge University Press. 2003
Thorough and clear coverage of microarray design, construction, image proc, and normalization. What caught my eye was the chapter on oilgo design, but its all good. Best single book on microarrays I’ve seen.

Bioinformatics: Methods and Protocols
Edited by Stephen Misener, Stephen A. Krawetz
Humana Press; 1st edition 2000
Program based by chapter. Too program based for a course. Has good chpaters on Clustal and Phylip. A chapter on Trascription control regions using MatInspector/GenomeInspector, weight matrix based sequence scanning for single or paired binding sites.

Computational Molecular Biology: an Algorithmic Approach
by Pavel A. Pevzner
MIT Press, 2000
Takes a unique approach. Looks at interesting computational aspects of seqeunce-based biology, and sometimes takes an odd sideways view of problems, getting deep into the underlying mathematics. A great complement to a more straightforward survey book. The topic coverage isn’t broad enough for my course, and the topics get covered in more depth than I need. Runs thorugh algorithmics of restircition digests to microarrays including, of course, sequencing by hybridization. Covers algorithmics of genomic comparisons. Great source book for a serious comp bio student.

DNA Microarrays: A Practical Approach
Edited by Mark Schena
Oxford University Press, Oxford, UK, 1999
A book on microarray technology. From DNA spotted on glass to enzymatic oligo arrays to ink jets, to microelectronic arrays. Written early on when many different approaches were being explored. Great source for technical information.

Mathematics of Genome Analysis
by Jerome K. Percus
Cambridge University Press; 1st edition 2002
Not a genomics book, but a mathmatician’ s look at DNA sequence, from clone libraries through seq alignments.

Post-genome Informatics
by Minoru Kanehisa
Oxford University Press, Oxford, 2000
Cool cover! Written by the guy behind KEGG. An eclectic choice of topics, first databases, then sequence analysis basics, then network analysis. Had a few pages on comparing networks that I found useful.

Guide to Analysis of DNA Microarray Data
by Steen Knudsen
John Wiley and Sons, New York, 2002
A what-to-do book on microarray data analysis. Very short, too short to explain how to do things, but describes what to do, issues to consider, and what results will look like. Useful as a place to start, will show you what you don’t know. The linked site has example R and BioConductor code.

Methods of Microarray Data Analysis II
Edited by Simon M. Lin and Kimberly F. Johnson
Springer, 2002
Papers from CAMDA ‘01 Various array analysis, especially advanced clsutering methods. Particularly interesting are:

  • Biology-Driven Clustering of Microarray Data; K.R. Coombes, et al.
    GO-based clustering.
  • Analysis of Gene Expression Profiles and Drug Activity Patterns by Clustering and Bayesian Network Learning; Jeong-Ho Chang, et al.
  • Topomap and bayesian clustering

DNA Arrays: Technologies and Experimental Strategies
Edited by Elena V. Grigorenko
CRC Press, 2001
What caught my eye are the technology chapters, one on oligo arrays and another on electrochemical array detection.

DNA Arrays: Methods and Protocols
Edited by Jang B. Rampal
Humana Press, 2001
This is another array technology book. Great information on ink-jet and photolithographic oligo synthesis. There are several sequencing by hybridization articles. It starts with a chapter on the history of the field by Southern. Great book for a collection of articles!

Primate life spans

Monday, March 14th, 2005

Googling for AcePerl tutorials (there has to be a better way to use AcePerl than what I’ve been doing!) , I happened across a list of primate lifespans. List has 239 primates. The winners are the great apes, with some monkeys having lifespans nearly as long, at a guess not really different given the sparsity of the data. Would be interesting to plot lifespans on a phylogram.

The Life Spans of Nonhuman Primates

Species                                                   Life Span
	
Allenopithecus nigroviridis (Allen's Swamp Monkey)        28 yrs. (1)
Allocebus trichotis (Hairy-eared Dwarf Lemur)             NA
Alouatta belzebul (Red-handed Howler)                     NA
Alouatta caraya (Black-and-gold Howler)                   20 yrs. (2)
Alouatta coibensis (Coiba Island Howler)                  NA
Alouatta fusca (Brown Howler)                             NA
Alouatta palliata (Mantled Howler)                        20 yrs. (1)
Alouatta pigra (Black Howler)                             20 yrs. (1)
Alouatta sara (Bolivian Red Howler)                       NA
Alouatta seniculus (Red Howler)                           25 yrs. (1)
Aotus nigriceps (Southern Red-necked Night Monkey)        20 yrs. (1)
Aotus trivigratus (Northern Gray-necked Owl Monkey)       20 yrs. (1)
Arctocebus aureus (Golden Angwantibo)                     13 yrs. (3)
Arctocebus calabarensis (Angwantibo)                      11 yrs. (1)
Ateles belzebuth (White-bellied Spider Monkey)            20 yrs. (1)
Ateles chamek (Black-faced Spider Monkey)                 40 yrs. (3)
Ateles fusciceps (Brown-headed Spider Monkey)             24 yrs. (1)
Ateles geoffroyi (Black-handed Spider Monkey)             48 yrs. (3)
Ateles marginatus (White-whiskered Spider Monkey)         NA
Ateles paniscus (Black Spider Monkey)                     33 yrs. (1)
Avahi laniger (Woolly Lemur)                              NA
Brachyteles arachnoides (Woolly Spider Monkey or
    Muriqui)                                              30 yrs. (1)
Bunopithecus [Hylobates] hoolock (Hoolock                 42 yrs. (1)
    or White-browed Gibbo
Cacajao calvus (Bald Uacari)                              20.1 yrs. (1)
Cacajao melanocephalus (Black-headed Uacari)              18 yrs. (2)
Callicebus brunneus (Brown Titi Monkey)                   NA
Callicebus caligatus (Chestnut-bellied Titi Monkey)       NA
Callicebus cinerascens (Ashy Titi Monkey)                 NA
Callicebus cupreus (Red Titi Monkey)                      NA
Callicebus donacophilus (Bolivian Gray Titi Monkey)       NA
Callicebus dubius (Titi Monkey)                           NA
Callicebus hoffmannsi (Hoffman's Titi Monkey)             NA
Callicebus modestus (Titi Monkey)                         NA
Callicebus moloch (Dusky Titi Monkey)                     25 yrs. (2)
Callicebus oenanthe (Andean Titi Monkey)                  NA
Callicebus olallae (Beni Titi Monkey)                     NA
Callicebus personatus (Masked Titi Monkey)                NA
Callicebus torquatus (Collared Titi or Widow Monkey)      NA
Callimico goeldii (Goeldi's Monkey)                       17.9 yrs. (1)
Callithrix argentata (Bare-ear Marmoset)                  17 yrs. (2)
Callithrix aurita (Buffy Tufted-eared Marmoset)           NA
Callithrix flaviceps (Buffy-headed Marmoset)              NA
Callithrix geoffroyi (Geoffroy's Tufted-eared Marmoset)   NA
Callithrix humeralifer (Tassel-eared Marmoset)            15 yrs. (2)
Callithrix jacchus (Common Marmoset)                      11.7 yrs. (1)
Callithrix mauesi (Maues Marmoset)                        NA
Callithrix penicillata (Black Tufted-eared Marmoset)      NA
Callithrix pygmaea (Pygmy Marmoset)                       11.7 yrs. (1)
Callthrix kuhlii (Wied's Tufted-eared Marmoset)           NA
Callthrix nigriceps (Black-headed Marmoset)               NA
Cebus albifrons (White-fronted Capuchin)                  44 yrs. (1)
Cebus apella (Tufted or Brown Capuchin)                   40 yrs. (1)
Cebus capucinus (White-throated Capuchin)                 46.9 yrs. (1)
Cebus olivaceus (Weeper or Wedge-capped Capuchin)         NA
Cercocebus agilis (Agile Mangabey)                        NA
Cercocebus galeritus (Tana River Mangabey)                19 yrs. (1)
Cercocebus torquatus (White-collared Mangabey)            27 yrs. (1)
Cercocebus torquatus atys (Sooty Mangabey)                18 yrs. (1)
Cercopithecus campbelli (Campbell's Guenon)               25 yrs. (2)
Cercopithecus cephus (Mustached Guenon)                   22 yrs. (1)
Cercopithecus diana (Diana Monkey)                        34.8 yrs. (1)
Cercopithecus dryas (Dryas Guenon)                        NA
Cercopithecus erythrogaster (White-throated Guenon)       NA
Cercopithecus erythrotis (Red-eared Guenon)               NA
Cercopithecus hamlyni (Owl-faced Monkey)                  27 yrs. (2)
Cercopithecus lhoesti (L'Hoest's Monkey)                  NA
Cercopithecus mitis (Blue Monkey)                         20 yrs. (1)
Cercopithecus mona (Mona Monkey)                          22 yrs. (1)
Cercopithecus neglectus (De Brazza's Monkey)              22 yrs. (1)
Cercopithecus nictitans (Putty-nosed                      23 yrs. (2)
     or Greater Spot-nosed Guenon)
Cercopithecus petaurista (Lesser Spot-nosed Guenon)       19 yrs. (2)
Cercopithecus pogonias (Crowned Guenon)                   20 yrs. (1)
Cercopithecus preussi (Preuss's Monkey)                   NA
Cercopithecus sclateri (Sclater's Guenon)                 NA
Cercopithecus solatus (Sun-tailed Guenon)                 NA
Cercopithecus wolfi (Wolf's Guenon)                       NA
Cheirogaleus major (Greater Dwarf Lemur)                  8.8 yrs. (1)
Cheirogaleus medius (Fat-tailed Dwarf Lemur)              19 yrs. (2)
Chiropotes albinasus (White-nosed Bearded Saki)           12 yrs. (2)
Chiropotes satanas (Bearded Saki)                         15 yrs. (1)
Chlorocebus aethiops (Vervet, Grivet, or Green Monkey)    31 yrs. (1)
Colobus angolensis (Angolan Black-and-white Colobus)      NA
Colobus guereza (Abyssinian, Guereza, or
    Eastern Black-and-white Colobus)                      22.2 yrs. (1)
Colobus polykomos (King or Western Black-and-white
    Colobus)                                              30.5 yrs. (1)
Colobus satanas (Black Colobus)                           NA
Colobus vellerosus (Geoffroy's or White-thighed
    Black-and-white colobus)                              NA
Daubentonia madagascariensis (Aye-aye)                    24 yrs. (2)
Erythrocebus patas (Patas Monkey)                         21.6 yrs. (1)
Eulemur coronatus (Crowned Lemur)                         NA
Eulemur fulvus (Brown Lemur)                              30.8 yrs. (1)
Eulemur macaco (Black Lemur)                              27.1 yrs. (1)
Eulemur mongoz (Mongoose Lemur)                           <26 yrs.  (4)
Eulemur rubriventer (Red-bellied Lemur)                   NA
Euoticus elegantulus (Southern Needle-clawed Bush Baby)   NA
Euoticus pallidus (Northern Needle-clawed Bush Baby)      NA
Galago alleni (Allen's Bush Baby)                         12 yrs. (1)
Galago gallarum (Somali Bush Baby)                        NA
Galago matschiei (Matschie's Bush Baby)                   NA
Galago moholi (Southern Lesser Bush Baby)                 16 yrs. (1)
Galago senegalensis (Northern Lesser Bush Baby)           16 yrs. (1)
Galagoides demidoff (Demidoff's Bush Baby)                13 yrs. (1)
Galagoides thomasi (Thomas's Bush Baby)                   NA
Galagoides zanzibaricus (Zanzibar Bush Baby)              16.5 yrs. (3)
Gorilla gorilla beringei (Mountain Gorilla)               40-50 yrs. (1)
Gorilla gorilla gorilla (Western Lowland Gorilla)         50 yrs. (1)
Gorilla gorilla graueri (Eastern Lowland Gorilla)         NA
Hapalemur aureus (Golden Bamboo Lemur)                    NA
Hapalemur griseus (Lesser Bamboo Lemur)                   17 yrs. (2)
Hapalemur simus (Greater Bamboo Lemur)                    NA
Hylobates agilis (Dark-handed or Agile Gibbon)            32 yrs. (1)
Hylobates klossi  (Kloss's Gibbon)                        NA
Hylobates lar (White-handed Gibbon)                       44 yrs. (1)
Hylobates moloch (Silvery Javan Gibbon)                   35 yrs. (1)
Hylobates muelleri (Mueller's Bornean Gray Gibbon)        47 yrs. (1)
Hylobates pileatus (Pileated or Capped Gibbon)            39 yrs. (1)
Indri indri (Indri)                                       NA
Kasi [Trachypithecus] vetulus (Purple-faced Leaf Monkey)  8 yrs. (4)
Kasi [Trachypithecus] johnii (Nilgiri Langur)             NA
Lagothrix flavicauda (Yellow-tailed Woolly Monkey)        NA
Lagothrix lagotricha (Woolly Monkey)                      25.9 yrs. (1)
Lemur catta (Ring-tailed Lemur)                           27 yrs. (1)
Leontopithecus caissara (Black-faced Lion Tamarin)        NA
Leontopithecus chrysomelas (Golden-headed Lion Tamarin)   NA
Leontopithecus chrysopygus (Black Lion Tamarin)           NA
Leontopithecus rosalia (Golden Lion Tamarin)              24 yrs. (2)
Lepilemur dorsalis (Gray-backed Sportive Lemur)           NA
Lepilemur edwardsi (Milne-Edwards' Sportive Lemur)        NA
Lepilemur leucopus (White-footed Sportive Lemur)          NA
Lepilemur microdon (Small-toothed Sportive Lemur)         NA
Lepilemur mustelinus (Weasel Sportive Lemur)              NA
Lepilemur ruficaudatus (Red-tailed Sportive Lemur)        NA
Lepilemur septentrionalis (Northern Sportive Lemur)       NA
Lophocebus albigena (Gray-cheeked Mangabey)               32.6 yrs. (1)
Lophocebus aterrimus (Black Mangabey)                     32.7 yrs. (3)
Loris tardigradus (Slender Loris)                         15 yrs. (1)
Macaca arctoides (Stump-tailed Macaque)                   30 yrs. (1)
Macaca assamensis (Assamese Macaque)                      NA
Macaca cyclopis (Formosan Rock Macaque)                   NA
Macaca fascicularis (Long-tailed, Crab-eating or
    Cynomolgus Macaque)                                   37.1 yrs. (1)
Macaca fuscata (Japanese Macaque)                         33 yrs. (1)
Macaca maura (Celebes Moor Macaque)                       NA
Macaca mulatta (Rhesus Macaque)                           29 yrs. (1)
Macaca nemestrina (Pig-tailed Macaque)                    26.3 yrs. (1)
Macaca nigra (Celebes or Crested Black)                   18 yrs. (1)
Macaca ochreata (Booted Macaque)                          NA
Macaca radiata (Bonnet Macaque)                           30 yrs. (1)
Macaca silenus (Lion-tailed Macaque)                      38 yrs. (1)
Macaca sinica (Toque Macaque)                             30 yrs. (1)
Macaca sylvanus (Barbary Macaque)                         22 yrs. (1)
Macaca thibetana (Tibetan Macaque)                        20 yrs. (1)
Macaca tonkeana (Tonkean Macaque)                         NA
Mandrillus leucophaeus (Drill)                            46 yrs. (4)
Mandrillus sphinx (Mandrill)                              46.3 yrs. (1)
Microcebus coquereli (Coquerel's Dwarf Lemur)             15 yrs. (2)
Microcebus murinus (Gray Mouse Lemur)                     15.5 yrs. (1)
Microcebus myoxinus (Pygmy Mouse Lemur)                   NA
Microcebus rufus (Brown Mouse Lemur)                      NA
Miopithecus talapoin (Dwarf Guenon or Southern
    Talapoin Monkey)                                      27.7 yrs. (1)
Nasalis [Nasalis] larvatus (Proboscis Monkey)             21 yrs. (2)
Nomascus [Hylobates] leucogenys (Chinese
    White-cheeked Gibbon)                                 28 yrs. (1)
Nomascus [Hylobates] gabriellae (Golden-cheeked Gibbon)   46 yrs. (1)
Nycticebus coucang (Slow Loris)                           20 yrs. (1)
Nycticebus pygmaeus (Pygmy Loris)                         20 yrs. (1)
Otolemur crassicaudatus (Thick-tailed Greater Bush Baby)  15 yrs. (1)
Otolemur garnettii (Garnett's Greater Bush Baby)          15 yrs. (1)
Pan paniscus (Bonobo or Pygmy Chimpanzee)                 40 yrs. (1)
Pan troglodytes (Chimpanzee)                              53 yrs. (1)
Papio hamadryas anubis (Olive Baboon)                     30-45 yrs. (1)
Papio hamadryas cynocephalus (Yellow Baboon)              40 yrs. (1)
Papio hamadryas hamadryas (Hamadryas Baboon)              35.6 yrs. (1)
Papio hamadryas papio (Guinea Baboon)                     40 yrs. (1)
Papio hamadryas ursinus (Chacma Baboon)                   45 yrs. (1)
Perodicticus potto (Potto)                                26 yrs. (1)
Phaner furcifer (Fork-marked Lemur)                       12 yrs. (2)
Piliocolobus [Procolobus] pennantii (Pennant's Red
    Colobus)                                              NA
Piliocolobus [Procolobus] preussi (Preuss's Red Colobus)  NA
Piliocolobus [Procolobus] rufomitratus (Tana River
    Red Colobus)                                          NA
Piliocolobus [Procolobus] baduis (Western Red Colobus)    NA
Pithecia aequatorialis (Equatorial Saki)                  NA
Pithecia albicans (Buffy Saki)                            NA
Pithecia irrorata (Bald-faced Saki)                       NA
Pithecia monachus (Monk Saki)                             25 yrs. (2)
Pithecia pithecia (White-faced Saki)                      35 yrs. (3)
Pongo abelii (Sumatran Orangutan)                         >50 yrs. (1)
Pongo pygmaeus (Borneo Orangutan)                         59 yrs. (1)
Presbytis comata (Grizzled Leaf Monkey)                   NA
Presbytis femoralis (Banded Leaf Monkey)                  NA
Presbytis frontata (White-fronted Leaf Monkey)            NA
Presbytis hosei (Hose's Leaf Monkey)                      NA
Presbytis melalophos (Mitered Leaf Monkey)                16 yrs. (2)
Presbytis potenziani (Mentawai Island Leaf Monkey)        NA
Presbytis rubicunda (Maroon Leaf Monkey)                  NA
Presbytis thomasi (Thomas's Leaf Monkey)                  NA
Procolobus [Procolobus] verus (Olive Colobus)             NA
Propithecus diadema (Diademed Sifaka)                     20 yrs. (1)
Propithecus tattersalli (Golden-crowned Sifaka)           NA
Propithecus verreauxi (Verreaux's Sifaka)                 20 yrs. (2)
Pygathrix [Pygathrix] nemaeus (Red-shanked Douc Langur)   >30 yrs. (1)
Pygathrix [Pygathrix] nigripes (Black-shanked Douc
    Langur)                                               NA
Rhinopithecus [Pygathrix) roxellana
(Sichuan Golden Snub-nosed Monkey)                        NA
Rhinopithecus [Pygathrix] avunculus (Tonkin
    Snub-nosed Monkey)                                    NA
Rhinopithecus [Pygathrix] bieti (Black or Yunnan
    Snub-nosed Monkey)                                    NA
Rhinopithecus [Pygathrix] brelichi (Guizhou
    Snub-nosed Monkey)                                    NA
Saguinus bicolor (Bare-faced Tamarin)                     8 yrs. (1)
Saguinus fuscicollis (Saddleback Tamarin)                 24 yrs. (2)
Saguinus geoffroyi (Red-crested Tamarin)                  13 yrs. (1)
Saguinus imperator (Emperor Tamarin)                      17 yrs. (1)
Saguinus inustus (Mottled-face Tamarin)                   NA
Saguinus labiatus (Red-bellied Tamarin)                   NA
Saguinus leucopus (Silvery-brown Bare-faced Tamarin)      NA
Saguinus midas (Golden-handed Tamarin)                    13.2 yrs. (1)
Saguinus mystax (Mustached Tamarin)                       12-20 yrs. (1)
Saguinus nigricollis (Spix's Black-mantled Tamarin)       13.9 yrs. (1)
Saguinus oedipus (Cotton-top Tamarin)                     13.5 yrs. (1)
Saguinus tripartitus (Golden-mantled Saddleback Tamarin)  6 yrs. (1)
Saimiri boliviensis (Bolivian Squirrel Monkey)            NA
Saimiri oerstedii (Red-backed Squirrel Monkey)            NA
Saimiri sciureus (Common Squirrel Monkey)                 21 yrs. (1)
Saimiri ustus (Golden-backed Squirrel Monkey)             NA
Saimiri vanzolinii (Black Squirrel Monkey)                NA
Semnopithecus entellus (Hanuman Langur)                   20 yrs. (1)
Simias [Nasalis] concolor (Pig-tailed Langur)             NA
Symphalangus [Hylobates] syndactylus (Siamang)            35yrs. (1)
Tarsius bancanus (Western Tarsier)                        8-12 yrs. (1)
Tarsius pumilus (Pygmy Tarsier)                           NA
Tarsius spectrum (Spectral Tarsier)                       12 yrs. (1)
Tarsius syrichta (Phillippine Tarsier)                    13.5 yrs. (1)
Tarsius dianae (Dian's Tarsier)                           NA
Theropithecus gelada (Gelada Baboon)                      19.2 yrs. (1)
Trachypithecus [Trachypithecus] auratus (Ebony Langur)    NA
Trachypithecus [Trachypithecus] cristatus (Silvered
    Langur)                                               31 yrs. (3)
Trachypithecus [Trachypithecus] delacouri (Delacour's
    Langur)                                               NA
Trachypithecus [Trachypithecus] francoisi (Francois's
    Langur)                                               <20 yrs. (4)
Trachypithecus [Trachypithecus] geei (Golden Langur)      NA
Trachypithecus [Trachypithecus] obscurus (Dusky or
    Spectacled Leaf Monkey)                               NA
Trachypithecus [Trachypithecus] phayrei (Phayre's Leaf
    Monkey)                                               NA
Trachypithecus [Trachypithecus] pileatus (Capped Leaf
    Monkey)                                               NA
Varecia variegatus (Ruffed Lemur)                         19 yrs. (1)

Numbers in parenthesus following lifespans refer to the following references:

1. Rowe, Noel. The Pictorial Guide to Living Primates. Pogonias Press, East Hampton, New York, 1996.
2. Hakeem A., et al. Handbook of the Psychology of Aging. 4th ed. Birren, J.E., Schaie, K.W., Editors. San Diego:
Academic Press. 1996.
3. Nowak, R. Walker’s Primates of the World. Johns Hopkins University Press, Baltimore, Maryland, 1999.
4. American Association of Zoo Keepers Greater San Francisco Bay Area Chapter. Biological Values for Selected
Mammals. Topeka: AAZK. 1992. 3rd ed. Pgs: v, 481

*The data presented here is taken from the secondary sources listed above and users are advised to consult primary
sources before citing this information. According to Rowe (1996, p. 6), “Species life span is given in years and
measures the maximum amount of time between birth and death rather than an average.” However, life span
information varies, as might be expected, from source to source. Moreover, the information provided is drawn mainly
from reports on captive animals. While it is generally assumed that captive animals will live longer than animals in
the wild, because of the consistent care and support provided in laboratory or zoo settings, according to Hakeem
et al.:

“We have very little information on the longevity of primates in the wild,
because this requires sustained observations of wild populations for many
decades. One of our concerns in using life spans of captive animals was that
they might vary greatly from the species — maximum life span in the wild; one
might think that primates living in zoos would have longer maximum life spans
than those living in the wild. The few very long-term studies of primates
living under natural conditions indicate, however, that some individuals do live
into extreme old age in the wild. Long-term observational data suggest that
the maximum life spans for zoo-living and wild primates may be about the
same (p. 78-9).”

Anyone who would like to contribute verifiable information about nonhuman primate life spans — especially for those
where information is not provided (NA) — should contact Ray Hamel at hamel@primate.wisc.edu.

Information compiled by Derek Johnson.

Tasmanian Tiger

Friday, March 4th, 2005

Here’s a site with films of the tasmanian tiger, the thylacine (Thylacinus cynocephalus). It was driven to extinction in the 1930’s.

mounted thylacine

Thylacine films

There’s interest in sequencing the genome of the tasmanian devil with an eye toward eventual cloning. Reconstructing a genome of an extinct species is currently not technically feasible. So far they have been able to clone short DNA segments from preserved tissue.