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Instance-based error correction for short reads of disease-associated genes
BACKGROUND: Genomic reads from sequencing platforms contain random errors. Global correction algorithms have been developed, aiming to rectify all possible errors in the reads using generic genome-wide patterns. However, the non-uniform sequencing depths hinder the global approach to conduct effecti...
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| Vydáno v: | BMC Bioinformatics |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2021
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8170817/ https://ncbi.nlm.nih.gov/pubmed/34078284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-021-04058-y |
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