A probabilistic framework for aligning paired-end RNA-seq data
Author(s) -
Yin Hu,
Kai Wang,
Xiaping He,
Derek Y. Chiang,
Jan F. Prins,
Jinze Liu
Publication year - 2010
Publication title -
bioinformatics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.599
H-Index - 390
eISSN - 1367-4811
pISSN - 1367-4803
DOI - 10.1093/bioinformatics/btq336
Subject(s) - splice , fragment (logic) , rna splicing , probabilistic logic , computational biology , exon , computer science , alternative splicing , genome , biology , genetics , rna , algorithm , gene , artificial intelligence
The RNA-seq paired-end read (PER) protocol samples transcript fragments longer than the sequencing capability of today's technology by sequencing just the two ends of each fragment. Deep sampling of the transcriptome using the PER protocol presents the opportunity to reconstruct the unsequenced portion of each transcript fragment using end reads from overlapping PERs, guided by the expected length of the fragment.
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