An heuristic filtering tool to identify phenotype-associated genetic variants applied to human intellectual disability and canine coat colors

BACKGROUND: Identification of one or several disease causing variant(s) from the large collection of variants present in an individual is often achieved by the sequential use of heuristic filters. The recent development of whole exome sequencing enrichment designs for several non-model species creat...

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Vydáno v:BMC Bioinformatics
Hlavní autoři: Broeckx, Bart J. G., Coopman, Frank, Verhoeven, Geert, Bosmans, Tim, Gielen, Ingrid, Dingemanse, Walter, Saunders, Jimmy H., Deforce, Dieter, Van Nieuwerburgh, Filip
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2015
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4656174/
https://ncbi.nlm.nih.gov/pubmed/26597515
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-015-0822-7
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