Open hejian41 opened 2 months ago
Single-cell RNA sequencing captures mRNA fragments from the polyA tail at the 3' end, making it challenging to recover longer sequences that can provide information about the originating transcript. To accurately quantify transcripts, methods like single-cell full-length capture or Smart-seq, which offer full-length coverage, may be required.
Got it. Thanks for your reply.
I'm not sure the BRIE2 can fulfill your need, https://genomebiology.biomedcentral.com/articles/10.1186/s13059-021-02461-5
Apologies for the delayed response. BRIE2 identify gene differentiation through spliced and unspliced states, not transcript variants. My objective is to assess gene targeting efficiency, given elements inserted into a specific gene transcript. Thank you for suggestion.
Hi Shuangshuang,
Considering a gene can produce multiple transcripts, is there a method to obtain a transcript counting matrix instead of a gene-based one during data preprocessing?
Thank you!