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Analysis of optimal alignments unfolds aligners’ bias in existing variant profiles
Efforts such as International HapMap Project and 1000 Genomes Project resulted in a catalog of millions of single nucleotides and insertion/deletion (INDEL) variants of the human population. Viewed as a reference of existing variants, this resource commonly serves as a gold standard for studying and...
Tallennettuna:
| Julkaisussa: | BMC Bioinformatics |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5073887/ https://ncbi.nlm.nih.gov/pubmed/27766935 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-016-1216-1 |
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