Abstract

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.
Original languageEnglish
Publication statusPublished - 2015
MoE publication typeI2 ICT software

Fields of Science

  • 113 Computer and information sciences
  • Bioinformatics

Cite this

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title = "Gap2Seq",
abstract = "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.",
keywords = "113 Computer and information sciences, Bioinformatics",
author = "Salmela, {Leena Maija} and Kristoffer Sahlin and M{\"a}kinen, {Veli Antti Tapani} and Tomescu, {Alexandru Ioan}",
year = "2015",
language = "English",

}

Gap2Seq. Salmela, Leena Maija (Author); Sahlin, Kristoffer (Author); Mäkinen, Veli Antti Tapani (Author); Tomescu, Alexandru Ioan (Author). 2015.

Research output: Non-textual formSoftwareScientific

TY - ADVS

T1 - Gap2Seq

AU - Salmela, Leena Maija

AU - Sahlin, Kristoffer

AU - Mäkinen, Veli Antti Tapani

AU - Tomescu, Alexandru Ioan

PY - 2015

Y1 - 2015

N2 - 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.

AB - 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.

KW - 113 Computer and information sciences

KW - Bioinformatics

M3 - Software

ER -