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An Alphabetic List of Genetic Analysis Software PAGE 1 (A-F) |
URL
master:
http://www.nslij-genetics.org/soft/
mirror:
http://linkage.rockefeller.edu/soft/
searchable database:
http://www.animalgenome.org/soft/ (NEW!)
Last Update:
September 05, 2008
| Computer software on the following topics are included here: genetic linkage analysis for human pedigree data, QTL analysis for animal/plant breeding data, genetic marker ordering, genetic association analysis, haplotype construction, pedigree drawing, and population genetics. This list is offered here as a service to the gene mapping community. The inclusion of a program should not be interpreted as an endorsement to that program from us. |
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This page was created by Dr. Wentian Li, when he was
at Columbia University (1995-1996). It was later
moved to Rockefeller University (1996-2002), and now
takes its new home at North Shore LIJ Research
Institute (2002-now). More than 240 programs have
been listed by December 2004, more than 350
programs by August 2005, close to 400 programs by December 2006,
and close to 460 programs by June 2008.
A version of the searchable database was developed by
Zhiliang Hu of Iowa State University, and a recent round
of updating was assisted by Wei JIANG of Harbin Medical School.
Some earlier software can be downloaded from EBI: ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/ (Linkage and Mapping Software Repository), and http://genamics.com/software/index.htm may contain archived copy of some programs. If you have new programs to add or any updated information, please send a message to webadm@nslij-genetics.org |
what's new |
link to other sources |
obsolete programs
page 1 (A-F) |
page 2 (G-L) |
page 3 (M-P) |
page 4 (Q-Z)
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[x]
[y]
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http://www.epigenetic.org/Linkage/act.tar.gz
Amos (1994), "Robust variance-components approach for assessing genetic
linkage in pedigrees",
American Journal of Human Genetics, 54:535-543.
[abstract]
de Andreade, Amos, Thiel (1999),
"Methods to estimate genetic parameters for quantitative traits",
Genetic Epidemiology, 17(1):64-76.
CJ Hoggart, MD Shriver, RA Kittles, DG Clayton, PM McKeigue (2004),
"Design and analysis of admixture mapping studies",
American Journal of Human Genetics, 74(5):965-978.
[html]
CJ Hoggart, EJ Parra, MD Shriver, C Bonilla, RA Kittles, DC Clayton, PM McKeigue
(2003), "Control of confounding of genetic associations in stratified
populations",
American Journal of Human Genetics, 72(6):1492-1504.
[html]
PM McKeigue, J Carpenter, EJ Parra, MD Shriver (2000),
"Estimation of admixture and detection of linkage in admixed populations
by a Bayesian approach: application to African-American populations",
Annals of Human Genetics, 64:171-186.
Gudbjartsson, Jonasson, Frigge, Kong (2000)
"Allegro, a new computer program for multipoint linkage analysis",
Nature Genetics, 25:12-13.
Gudbjartsson, Thorvaldsson, Gunnarsson, Kong, Ingolfsdottir (2004),
"Decision diagram based multipoint linkage analysis: ALLEGRO2",
American Journal of Human Genetics, 75(suppl):?.
Gudbjartsson, Thorvaldsson, Kong, Gunnarsson, Ingolfsdottir (2005),
"Allegro version 2",
Nature Genetics, 37:1015-1016.
[PLEASE CITE THIS REFERENCE WHEN USING THE ALLEGRO2 PROGRAM]
ftp://ftp.hgu.mrc.ac.uk/pub/ALP
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/linkage_cpmc_columbia/analyze/
[PDF]
"man pages"
http://lgb.unige.ch/arlequin/
Schneider, Kueffer, Roessli, Excofier, "Arlequin: A software for
population genetic data analysis. Ver 1.1",
(Genetics and Biometry Lab, Dept. of Anthropology, University of
Geneva, 1997);
User's manual (PDF, v1.1)
User's manual (PDF, v3.1)
previously:
ftp://lahmed.stanford.edu/pub/aspex
online manual (PDF)
Beaumont, Balding (2004), "Identifying adaptive genetic divergence among
populations from genome scans", Molecular Ecology, 13:969-980.
Browning BR and Browning SR (2007),
"Efficient multilocus association testing for whole genome association
studies using localized haplotype clustering",
Genetic Epidemiology, 31:365-375.
http://www.fas.harvard.edu/~junliu/TechRept/03folder/bladev2.tgz
Lu, Niu, Liu (2003),
"Haplotype information and linkage disequilibrium mapping for
single nucleotide polymorphisms", Genome Research, 13:2112-2117.
or a copy from
http://hpcio.cit.nih.gov/lserver/BLOCK.html
ftp://ftp.cs.auc.dk/pub/packages/block/current
http://www.geneticepi.com/Research/software/booLD-1.1.tar.gz
ftp://ftp.u.washington.edu/pub/user-supported/pangaea/PANGAEA/BOREL
Givry, Bouchez, Chabrier, Milan, Schiex (2005),
"CARTHAGENE: multipopulation integrated genetic and
radiation hybrid mapping",
Bioinformatics, 21(8):1703-1704.
ftp://fastlink.nih.gov/pub/caspar
Buhler, et. al. (1997)
Human Heredity,
47(4):211-222.
Satten, Epstein (2004), "Comparison of prospective and retrospective
methods for haplotype inference in case-control studies",
Genetic Epidemiology, 27(3):192-201
http://www.smd.qmul.ac.uk/statgen/software/dcurtis/chhet10.zip
Sun, Levin, Boerwinkle, Robertson, Kardia (2006),
"A scan statistic for identifying chromosomal patterns of SNP association",
Genetic Epidemiology, 30(7):627-635.
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
http download:
https://sourceforge.net/project/showfiles.php?group_id=27707
Devlin, Jones, Bacanu, Roeder (2002),
"Reply to Olson",
Genetic Epidemiology, 23(4):449-455.
documentation (version 2.4, 1990).
Tutorial (from biobase.dk)
http://www.cyrillicsoftware.com/download/downloads.htm
http://www.biostat.harvard.edu/~ileykin/accessory.htm
Yahoo discussion group:
http://groups.yahoo.com/group/dchip/
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
http://sourceforge.net/projects/easylinkage/
Hoffmann, Lindner (2005),
"easyLINKAGE-Plus - automated linkage analyses using large-scale SNP data"
Bioinformatics, 21(17):3565-3567.
based on some earlier prototype routines by Jochen Kumm.
http://www.stat.washington.edu/thompson/Genepi/Eclipse.shtml
Gu, Rao (1997), "A linkage strategy for detection of human quantitative-trait loci:
I. Generalized relative risk ratios and power of sib pairs with extreme trait values",.
American Journal of Human Genetics, 61(1):200-210.
[abstract]
Gu, Rao (1997),
"A linkage strategy for detection of human quantitative-trait loci:
II. Optimization of study designs based on extreme sib pairs and generalized relative
risk ratios",
American Journal of Human Genetics, 61(1):211-222.
[abstract]
http://www.genemapping.cn/eh.zip
online user's guide
a product review from:
http://www.scienceboard.net/resources/prodreviews.asp?cat=22&product=440
http://genepath.med.harvard.edu/~reich/EIGENSTRAT.htm
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
ftp://wpicf.wpic.pitt.edu/WPICCompgen/ettdt/index.html
Becker, Knapp (2004), "A powerful strategy to account for multiple testing in
the context of haplotype analysis",
American Journal of Human Genetics, 75:561-570.
[html]
Becker, Knapp (2005), "Impact of missing genotype data on
Monte-carlo simulation based haplotype analysis",
Human Heredity,
59:185-189.
Becker, Cichon, Jönson, Knapp (2005),
"Multiple testing in the context of haplotype analysis revisited:
application to case-control data",
Annals of Human Genetics, 69:1-10
Becker, Schumacher, Cichon, Baur, Knapp (2005),
"Haplotype interaction analysis of unlinked regions",
Genetic Epidemiology, 29:313-322.
Becker, Valentonyte, Croucher, Strauch, Schreiber, Hampe, Knapp (2006),
"Identification of probable genotyping errors by consideration of haplotypes",
European Journal of Human Genetics, 14:450-8.
Becker, Baur, Knapp (2006),
"Detection of parent-of-origin effects using haplotype analysis",
Human Heredity, 62:64-76
S Gerber, P Chabrier, A Kremer (2003), "FaMoz: a software for parentage
analysis using dominant, codominant and uniparentally inherited markers",
Molecular Ecology Notes, 3(3):479-481.
collarorators for version 4: Ann Becker, Dan Geiger.
ftp://fastlink.nih.gov/pub/fastlink (since Aug 6, 1996)
or
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/FASTLINK/fastlink
Schaffer, Gupta, Shriram, Cottingham (1994),
"Avoiding recomputation in linkage analysis",
Human Heredity, 44:225-237.
( PDF)
online README files (version 3.0P, december 95).
Dwarkadas, Schaffer, Cottingham, Cox, Keleher, Zwaenepoel,
"Parallelization of general linkage analysis problems",
( PDF)
Gupta, Schaffer, Cox,Zwaenepoel,
"Integrating parallelization strategies for linkage analysis",
( PDF)
Schaffer, "Faster linkage analysis computations for pedigrees with loops
or unused alleles",
( PDF)
Becker, Geiger, Schaffer, "Automatic selection of loop
breakers for genetic linkage analysis",
Human Heredity,
( PDF)
Becker, Bar-Yehuda, Geiger,
"Random algorithms for the loop cutset problem",
( PDF)
Schaffer, "Loops in FASTLINK",
( PDF)
Schaffer, "The mystery of (the) unknown",
( PDF)
Schaffer, "Pedigree traversal in FASTLINK",
( PDF)
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
registration page at:
http://watson.hgen.pitt.edu/register
online manual pages (same as slink)
Laird, Horvath, Xu (2000), Implementing a unified approach to family
based tests of association, Genetic Epi, supp 1, 19:36-42;
Rabinowitz, Laird (2000), A unified approach to adjusting association tests for
population admixture with arbitrary pedigree structure and arbitrary missing
marker information,
Human Heredity, 50:211-223.
Horvath, Xu, Laird (2001),
The family based association test method: strategies for studying general
genotype-phenotype associations, European J Hum Genet. 9:301-306.
http://finetti.meb.uni-bonn.de/ (graphic part, 2008 version)
http://ihg.gsf.de/linkage/download/finetti.zip (graphic part, 2004 version)
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
http://swfsc.noaa.gov/textblock.aspx?Division=FED&id=3442