טוען...
NeatFreq: reference-free data reduction and coverage normalization for De Novo sequence assembly
BACKGROUND: Deep shotgun sequencing on next generation sequencing (NGS) platforms has contributed significant amounts of data to enrich our understanding of genomes, transcriptomes, amplified single-cell genomes, and metagenomes. However, deep coverage variations in short-read data sets and high seq...
שמור ב:
| הוצא לאור ב: | BMC Bioinformatics |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4245761/ https://ncbi.nlm.nih.gov/pubmed/25407910 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-014-0357-3 |
| תגים: |
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