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Pakket: stringtie (2.2.1+ds-2)

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assemble short RNAseq reads to transcripts

The abundance of transcripts in a human tissue sample can be determined by RNA sequencing. The exact sequence sampled may be random, depending on the technology used. And it may be short, i.e. shorter than the transcript. At some point, many shorter reads need to be assembled to the model the complete transcripts.

StringTie knows how to assemble of RNA-Seq into potential transcripts without the need of a reference genome and provides a quantification also of the splice variants.

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stringtie downloaden

Pakket downloaden voor alle beschikbare platforms
Platform Pakketgrootte Geïnstalleerde grootte Bestanden
amd64 387,2 kB997,0 kB [overzicht]
arm64 337,6 kB937,0 kB [overzicht]
armel 334,3 kB952,0 kB [overzicht]
armhf 342,1 kB664,0 kB [overzicht]
i386 418,0 kB1.244,0 kB [overzicht]
mips64el 348,1 kB1.159,0 kB [overzicht]
mipsel 349,4 kB1.176,0 kB [overzicht]
ppc64el 401,3 kB1.245,0 kB [overzicht]
s390x 350,1 kB1.053,0 kB [overzicht]