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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:BMC Bioinformatics
Autors principals: Broeckx, Bart J. G., Coopman, Frank, Verhoeven, Geert, Bosmans, Tim, Gielen, Ingrid, Dingemanse, Walter, Saunders, Jimmy H., Deforce, Dieter, Van Nieuwerburgh, Filip
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2015
Matèries:
Software
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars