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MALVA: Genotyping by Mapping-free ALlele Detection of Known VAriants
The amount of genetic variation discovered in human populations is growing rapidly leading to challenging computational tasks, such as variant calling. Standard methods for addressing this problem include read mapping, a computationally expensive procedure; thus, mapping-free tools have been propose...
Tallennettuna:
| Julkaisussa: | iScience |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Elsevier
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6664100/ https://ncbi.nlm.nih.gov/pubmed/31352182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.isci.2019.07.011 |
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