Open ChoiJi-Hye opened 2 years ago
Hi @c-mertes , I am having the same issue:
Error in mergeNamedAtomicVectors(seqlengths(x), seqlengths(y), what = c("sequence", :
sequence chrM has incompatible seqlengths:
- in 'x': 16569
- in 'y': 16571
My genome index was built using GRCh37.primary_assembly.genome.fa
and gencode.v40lift37.annotation.gtf
using the following:
STAR --runThreadN 10 --runMode genomeGenerate --genomeDir genome --genomeFastaFiles /data/genome/GRCh37.primary_assembly.genome.fa --sjdbGTFfile /data/genome/gencode.v40lift37.annotation.gtf --sjdbOverhang 100
My FASTQ (paired-end) were aligned to this index to obtain the BAMs used in FRASER using the following code:
STAR --genomeDir /data/blood/genome/genome --readFilesIn "$i"_1.fastq.gz "$i"_2.fastq.gz --runThreadN 16 --readFilesCommand zcat --outSAMtype BAM SortedByCoordinate --chimSegmentMin 20 --quantMode GeneCounts --outReadsUnmapped Fastx --outFileNamePrefix ./star_out/"$i" --twopassMode Basic --outMultimapperOrder Random --sjdbGTFfile /data/blood/genome/gencode.v40lift37.annotation.gtf
Then, I followed the FRASER vignette but got to the same error as @ChoiJi-Hye . I am using Bioconductor version: Release (3.15). I appreciate any feedback. Thank you.
Hi.
I follow vignette with my bam file.
However, When I entered annotateRangesWithTxDb (fds, txdb=txdb, orgDb=orgDb), i got warning and error message : 403 genes were dropped because they have exons located on both strands of the same reference sequence or on more than one reference sequence, so cannot be represented by a single genomic range. Use 'single.strand.genes.only=FALSE' to get all the genes in a GRangesList object Error in mergeNamedAtomicVectors(seqlengths(x), seqlengths(y), what=c("seqeunce", : sequence chrM has incompatible seqlengths: - in 'x' : 16569 - in 'y' : 16571
I don't know what I can do with the fds object and how I can solve the problem. Thank you for your help.