Sammanfattning

Gap2Seq is a program for filling gaps in scaffolds produced by genome assembly tools using short read data such as reads produced by Illumina sequencing.
Originalspråkengelska
StatusPublicerad - 2015
MoE-publikationstypI2 ICT-programvara

Vetenskapsgrenar

  • 113 Data- och informationsvetenskap

Citera det här