Closed Bank-tidy closed 10 months ago
Could you please provide the head 1000 line of tomato_hifi.fill.paf ?
@cchd0001 Of course, thank you,but this file is a bit big. The first 10 lines of the file have reached 70M. If it is convenient, I can send it to you by email?
Oh, please do not use-a
for minimap2 because it set the output format as SAM ( but we expect PAF ).
Please change
--minmap_arg '-ax map-hifi -t 10 -K 80M'
to
--minmap_arg '-x map-hifi -t 10 -K 80M'
@cchd0001 Oh, I understand, thank you for your answer!
Dear Developer,
Thank you for creating this practical software. I've encountered a memory issue while using it and would like to consult you. Here is my code:
Initially, I input the complete genome sequence. The pipe.error file displays:
tgsgapcloser: line 645: 16242 Aborted (core dumped)$GapCloser --ont_reads_a $FINAL_READS --contig2ont_paf $OUT_PREFIX.fill.paf --min_match=$MIN_MATCH --min_idy=$MIN_IDY --prefix $OUT_PREFIX > $OUT_PREFIX.fill.log 2>&1
Following your suggestion of 5.5Gb xxx.paf records a 32Gb peak memory, I extracted the chromosome 7 genome with gap regions, resulting in a paf file of only 6.8G. My server has 512G of running memory, but I still encounter an error:
tgsgapcloser: line 645: 16242 Aborted (core dumped)$GapCloser --ont_reads_a $FINAL_READS --contig2ont_paf $OUT_PREFIX.fill.paf --min_match=$MIN_MATCH --min_idy=$MIN_IDY --prefix $OUT_PREFIX > $OUT_PREFIX.fill.log 2>&1
Should I reduce the -t parameter to 10 and increase the -K parameter to 80M, or do you have any other suggestions?The additional noteworthy point is that in the hifi.fill.log, it shows: "tgsgapcloser: ../biocommon/align_common/align_result.cpp:134: void BGIQD::ALIGN_COMMON::ExtraInfo::InitFromStr(const string&): Assertion `items.size() == 3' failed."
Here is my log screenshot
Best regards!