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Tool: Pintron: Gene-Structure Prediction Based On Spliced Alignments Of Transcript Sequences

PIntron is a tool for computing the exon/intron structure and the full-length isoforms of a genomic regions from a set of transcripts and the genomic sequence.

It computes the splicing alignments of the transcripts against the reference genome, it amalgamates the alignments to compute the exon-intron structure and then it computes the full-length isoforms.

PIntron is a command-line set of program that can be run on Linux 32/64 bit or Mac OS X. It is released under the open source AGPLv3 license.

The program (source code) and documentation can be found at http://www.algolab.eu/PIntron. To compile PIntron you need the usual GNU toolchain. To run it, you need Python and Perl.

Below is the the full-length isoforms computed on gene TP53.

The set of full-length isoforms for the gene TP53

pintron

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