Lataa...
Fastq2vcf: a concise and transparent pipeline for whole-exome sequencing data analyses
BACKGROUND: Whole-exome sequencing (WES) is a popular next-generation sequencing technology used by numerous laboratories with various levels of statistical and analytical expertise. Centralized databases, such as the Sequence Read Archive and the European Nucleotide Archive, allow data to be reanal...
Tallennettuna:
| Julkaisussa: | BMC Res Notes |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2015
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4376134/ https://ncbi.nlm.nih.gov/pubmed/25889517 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-015-1027-x |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|