Using familial information for variant filtering in high-throughput sequencing studies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/article/10.1007/s00439-014-1479-4/fulltext.html
Reference63 articles.
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2. Abecasis GR, Wigginton JE (2005) Handling marker–marker linkage disequilibrium: pedigree analysis with clustered markers. Am J Hum Genet 77:754–767. doi: 10.1086/497345
3. Abecasis GR, Cherny SS, Cookson WO, Cardon LR (2002) Merlin—rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97–101. doi: 10.1038/ng786
4. Aguiar D, Istrail S (2012) HapCompass: a fast cycle basis algorithm for accurate haplotype assembly of sequence data. J Comput Biol 19:577–590. doi: 10.1089/cmb.2012.0084
5. Albrechtsen A, Sand Korneliussen T, Moltke I, van Overseem Hansen T, Nielsen FC, Nielsen R (2009) Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium. Genet Epidemiol 33:266–274. doi: 10.1002/gepi.20378
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