Hi,
A quick question. You have the number of mismatches on a per
transcript basis in RefSeqAli for RefGenes correct ? Is there any way to
get the number of gaps/mismatches that were found in the alignment on a
per exon basis instead ?
Thank you,
--
Gabriel Renaud
Laboratório de Bioinformática e Biologia Computacional
Serviço de Pesquisa Clínica
Instituto Nacional de Câncer (INCA)
Rio de Janeiro - RJ
Tel.: +55-21-3233-1343
_______________________________________________
Genome maillist - [email protected]
https://lists.soe.ucsc.edu/mailman/listinfo/genome
