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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:
April 21, 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, and close to 400 programs by December 2006.
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
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obsolete programs
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.
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.
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, 72:1492-1504.
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]
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
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, 75:561-70.
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.
(see also VITESSE )
http://ihg.gsf.de/linkage/download/finetti.zip
ftp://ftp.ebi.ac.uk/pub/software/linkage_and_mapping/statgen/dcurtis/
http://swfsc.noaa.gov/textblock.aspx?Division=FED&id=3442
genetic analysis software list:
www.nslij-genetics.org/ga/soft
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