Closed lhui2010 closed 3 years ago
Hi Hui,
Sorry about that this repo make too rough, NOT detailed enough. The "isoseq_flnc.polyAtail.xls" have header not be print with classify_by_primer as following: "SeqName\tUMI\tSeqLength\tPolyALength\tPolyAtail". I was plan to publish the algorithm for IsoSeq data processing, isoform & polyA tail detection and quantifying, just not have much detail description on this repo, else, may can refer the methods section of our preprint in single cell isoseq also using the BGI patented RNA linking library preparation method (https://www.biorxiv.org/content/10.1101/2020.07.27.222349v1).
Hi Zhuoxing,
Thanks for the header and the paper link! Quite clear now! Looking forward for your paper! 👍
Best regards, Hui
Hi Zhuoxing,
Question
After classify_by_primer finished, three files seemed to be generated:
isoseq_flnc.polyAtail.xls
isoseq_nfl.fasta
isoseq_flnc.fasta
The two fasta files were easy to guess from their names, but what is the format of isoseq_flnc.polyAtail.xls? Is there a header or description of each column for it?
Also can you have a brief description on how classify_by_primer works?
Data
My Iso-Seq data was generated from
BGI patented multi-transcripts in one ZMW library
.Many thanks, Hui