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[ Source: stringtie  ]

Package: stringtie (3.0.3+ds-1)

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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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Download for all available architectures
Architecture Package Size Installed Size Files
amd64 463.5 kB1,152.0 kB [list of files]
arm64 393.9 kB1,132.0 kB [list of files]
armhf 398.9 kB811.0 kB [list of files]
i386 499.2 kB1,455.0 kB [list of files]
ppc64el 471.7 kB1,388.0 kB [list of files]
riscv64 435.0 kB852.0 kB [list of files]
s390x 476.6 kB1,244.0 kB [list of files]