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Indel detection from DNA and RNA sequencing data with transIndel
BACKGROUND: Insertions and deletions (indels) are a major class of genomic variation associated with human disease. Indels are primarily detected from DNA sequencing (DNA-seq) data but their transcriptional consequences remain unexplored due to challenges in discriminating medium-sized and large ind...
Tallennettuna:
| Julkaisussa: | BMC Genomics |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5909256/ https://ncbi.nlm.nih.gov/pubmed/29673323 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-018-4671-4 |
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