Project details for hapFabia

Screenshot hapFabia 1.4.2

by hochreit - December 28, 2013, 17:24:29 CET [ Project Homepage BibTeX BibTeX for corresponding Paper Download ]

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Description:

hapFabia identifies short identity by descent (IBD) segments that are tagged by rare variants in large sequencing data. Two haplotypes are identical by descent (IBD) if they share a segment that both inherited from a common ancestor. Current IBD methods reliably detect IBD segments longer than 1 Mbp (mega basepairs). hapFabia detects IBD segments in the range of 10 kbp (kilo basepairs). Many cohort studies contain unrelated individuals which share only short IBD segments. New sequencing techniques provide rare variants which convey more information on IBD than common variants, because random minor allele sharing of rare variants is less likely than for common variants.

Changes to previous version:

o citation update

o plot function improved

BibTeX Entry: Download
Corresponding Paper BibTeX Entry: Download
Supported Operating Systems: Agnostic
Data Formats: Agnostic
Tags: Bioinformatics, Sparsity, Biclustering, Genetics, Identity By Descent, Bayesian Optimization, Factor Analysis
Archive: download here

Other available revisons

Version Changelog Date
1.4.2

o citation update

o plot function improved

December 28, 2013, 17:24:29
1.4.1

o IBD lengths correction

o improved support for haploid genomes

November 8, 2013, 07:44:12
1.4.0

Initial Announcement on mloss.org.

October 20, 2013, 15:05:04

Comments

Sepp Hochreiter (on October 20, 2013, 15:05:54)
initial posting

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