Closed Xixu551 closed 5 months ago
I'm not sure about the contents of the returned final.bam file.
Judging from your error report, you need to build an index for final.bam and use samtools index
.
If your final.bam is not sorted, you have to use samtools sort
to sort.
I'm not sure about the contents of the returned final.bam file. Judging from your error report, you need to build an index for final.bam and use
samtools index
. If your final.bam is not sorted, you have to usesamtools sort
to sort.
Is there any arguments to let velocyto identify .bai file from 'samtools index'?
Sorry, only need samtools sort
Sorry, only need
samtools sort
I notice that the RNA velocity matrix in output directory has the following structure:
antisense.mtx.gz features.tsv.gz spliced.mtx.gz barcodes.tsv.gz spanning.mtx.gz unspliced.mtx.gz
Is there any thing I can do to convert it to .loom files so that it can be compatible with Scvelo's or Velocyto's python implemention?
我也有这个问题,请问您解决了吗
我想要运行velocyto,而华大仅返回了fastq文件和final.bam文件(约60GB),当我运行如下命令:
出现了如下报错: