טוען...
KvarQ: targeted and direct variant calling from fastq reads of bacterial genomes
BACKGROUND: High-throughput DNA sequencing produces vast amounts of data, with millions of short reads that usually have to be mapped to a reference genome or newly assembled. Both reference-based mapping and de novo assembly are computationally intensive, generating large intermediary data files, a...
שמור ב:
| Main Authors: | , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4197298/ https://ncbi.nlm.nih.gov/pubmed/25297886 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-881 |
| תגים: |
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