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Joining Illumina paired-end reads for classifying phylogenetic marker sequences
BACKGROUND: Illumina sequencing of a marker gene is popular in metagenomic studies. However, Illumina paired-end (PE) reads sometimes cannot be merged into single reads for subsequent analysis. When mergeable PE reads are limited, one can simply use only first reads for taxonomy annotation, but that...
Uloženo v:
| Vydáno v: | BMC Bioinformatics |
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| Hlavní autoři: | , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7071698/ https://ncbi.nlm.nih.gov/pubmed/32171248 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-020-3445-6 |
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