טוען...
TranscriptClean: variant-aware correction of indels, mismatches and splice junctions in long-read transcripts
MOTIVATION: Long-read, single-molecule sequencing platforms hold great potential for isoform discovery and characterization of multi-exon transcripts. However, their high error rates are an obstacle to distinguishing novel transcript isoforms from sequencing artifacts. Therefore, we developed the pa...
שמור ב:
| הוצא לאור ב: | Bioinformatics |
|---|---|
| Main Authors: | , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Oxford University Press
2019
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6329999/ https://ncbi.nlm.nih.gov/pubmed/29912287 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bty483 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|