Cargando…
Customisation of the Exome Data Analysis Pipeline Using a Combinatorial Approach
The advent of next generation sequencing (NGS) technologies have revolutionised the way biologists produce, analyse and interpret data. Although NGS platforms provide a cost-effective way to discover genome-wide variants from a single experiment, variants discovered by NGS need follow up validation...
Autores principales: | Pattnaik, Swetansu, Vaidyanathan, Srividya, Pooja, Durgad G., Deepak, Sa, Panda, Binay |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253117/ https://www.ncbi.nlm.nih.gov/pubmed/22238694 http://dx.doi.org/10.1371/journal.pone.0030080 |
Ejemplares similares
-
SInC: an accurate and fast error-model based simulator for SNPs, Indels and CNVs coupled with a read generator for short-read sequence data
por: Pattnaik, Swetansu, et al.
Publicado: (2014) -
A draft of the genome and four transcriptomes of a medicinal and pesticidal angiosperm Azadirachta indica
por: Krishnan, Neeraja M, et al.
Publicado: (2012) -
Customisation
por: Raich, U
Publicado: (1990) -
A customisable pipeline for the semi-automated discovery of online activists and social campaigns on Twitter
por: Primo, Flavio, et al.
Publicado: (2021) -
SIMPLEX: Cloud-Enabled Pipeline for the Comprehensive Analysis of Exome Sequencing Data
por: Fischer, Maria, et al.
Publicado: (2012)