Open JulioRogers opened 3 years ago
Hi,
Did you use nanopre ONT data as a .fastq?
Thanks
./minimap2 -ax map-ont reference.fasta BC10.fastq -o output.sam
Hi,
Did you use nanopre ONT data as a .fastq?
Thanks
Hello, thank you for your reply. Yes, I already used ONT, the problem is the same. I'm thinking that maybe the real problem is the file fastq.
Is reference.fasta file an assembled genome? Do you know how to further use .sam file after mapping the data on ONT?
Hi, I am using minimap2 (version: 2.20-r1061) with this cmd:
minimap2 -t 100 -k 2g -ax map-hifi -o out.sam ref.fa reads.fa
ref.fa file is a draft assembly, reads.fa file is HIFI reads. The mapping results is always "mapped (0.00% : N/A)", too. Do I need to use HIFI data as a .fastq? But there is nothing wrong when I use the .fasta file with ONT data or PacBio data. Could you please help me with this problem?
These are mapping result when the reads.fa is HIFI data.
11714594 + 0 in total (QC-passed reads + QC-failed reads) 0 + 0 secondary 0 + 0 supplementary 0 + 0 duplicates 0 + 0 mapped (0.00% : N/A) 0 + 0 paired in sequencing 0 + 0 read1 0 + 0 read2 0 + 0 properly paired (N/A : N/A) 0 + 0 with itself and mate mapped 0 + 0 singletons (N/A : N/A) 0 + 0 with mate mapped to a different chr 0 + 0 with mate mapped to a different chr (mapQ>=5)
These are mapping results when the reads.fa is ONT data (-ax map-ont) or PacBio data (-ax map-pb): ONT:
19158851 + 0 in total (QC-passed reads + QC-failed reads) 2834850 + 0 secondary 2734477 + 0 supplementary 0 + 0 duplicates 14992555 + 0 mapped (78.25% : N/A) 0 + 0 paired in sequencing 0 + 0 read1 0 + 0 read2 0 + 0 properly paired (N/A : N/A) 0 + 0 with itself and mate mapped 0 + 0 singletons (N/A : N/A) 0 + 0 with mate mapped to a different chr 0 + 0 with mate mapped to a different chr (mapQ>=5)
PacBio:
42914652 + 0 in total (QC-passed reads + QC-failed reads) 7130745 + 0 secondary 5973951 + 0 supplementary 0 + 0 duplicates 41004572 + 0 mapped (95.55% : N/A) 0 + 0 paired in sequencing 0 + 0 read1 0 + 0 read2 0 + 0 properly paired (N/A : N/A) 0 + 0 with itself and mate mapped 0 + 0 singletons (N/A : N/A) 0 + 0 with mate mapped to a different chr 0 + 0 with mate mapped to a different chr (mapQ>=5)
Hello everyone, I am using minimap2 with a fasta and a fastq files.
The line that I am trying is the following: ./minimap2 -ax map-ont reference.fasta BC10.fastq > output.sam
But the mapping result is always "mapped (0.00% : N/A)". I'm new in this area, and I don't know what could be the problem. Somebody could help me?