Fast alignment of reads to a variation graph with application to SNP detection
Sequencing technologies has provided the basis of most modern genome sequencing studies due to its high base-level accuracy and relatively low cost. One of the most demanding step is mapping reads to the human reference genome. The reliance on a single reference human genome could introduce substant...
I tiakina i:
| Ngā kaituhi matua: | , |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
De Gruyter
2021-11-01
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| Rangatū: | Journal of Integrative Bioinformatics |
| Ngā marau: | |
| Urunga tuihono: | https://doi.org/10.1515/jib-2021-0032 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
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