Hey!
Thank you for your great tool.
I am trying to use some 10X linked reads to improve the contig assembly of a _de _novo genome completed with oxford nanopore long reads. I first aligned the 10X reads with longranger and then continued from there.
Command:
/hpf/tools/centos7/Scaff10X/4.1/src/scaff10x -nodes 25 -bam /hpf/largeprojects/mdwilson/dustin/new_genome/phase_link/SUB_2626M1/outs/possorted_bam.bam genome.fa male_output.fasta
The "genome.fa" is the genome fasta file produced in the "refdata-assembly/fasta/" file made from longranger mkref.
The error specifically was:
Error running command: /hpf/tools/centos7/Scaff10X/4.1/src/scaff-bin/scaff_bwa-barcode tarseq.tag align0.dat align.dat > try.out
Try try-out file had this:
2751 409880285
Numbers of contigs: 2750 2751
Numbers of contigs are difference, please check reference assembly! 2750 2751
While not entirely sure what this meant, I did some digging and I noticed that one scaffold had 0 10-X reads aligning to it. Below is the summary of reads aligned per contig and the contig lacking reads.

I also noticed that the contig itself is on the shorter side.
Together, I have the following questions:
- Could the lack of alignment to a contig be responsible for this error?
- should there be a contig length cutoff in the inputted assembly?
- If this error is coming elsewhere, do you happen to know the source?
Thanks so much!
Dustin
Hey!
Thank you for your great tool.
I am trying to use some 10X linked reads to improve the contig assembly of a _de _novo genome completed with oxford nanopore long reads. I first aligned the 10X reads with longranger and then continued from there.
Command:
/hpf/tools/centos7/Scaff10X/4.1/src/scaff10x -nodes 25 -bam /hpf/largeprojects/mdwilson/dustin/new_genome/phase_link/SUB_2626M1/outs/possorted_bam.bam genome.fa male_output.fastaThe "genome.fa" is the genome fasta file produced in the "refdata-assembly/fasta/" file made from
longranger mkref.The error specifically was:
Error running command: /hpf/tools/centos7/Scaff10X/4.1/src/scaff-bin/scaff_bwa-barcode tarseq.tag align0.dat align.dat > try.outTry try-out file had this:
2751 409880285
Numbers of contigs: 2750 2751
Numbers of contigs are difference, please check reference assembly! 2750 2751
While not entirely sure what this meant, I did some digging and I noticed that one scaffold had 0 10-X reads aligning to it. Below is the summary of reads aligned per contig and the contig lacking reads.

I also noticed that the contig itself is on the shorter side.
Together, I have the following questions:
Thanks so much!
Dustin