Samtools index: failed to create index for
Web[E::hts_open_format] Failed to open file "1_ucheck.bam" : Exec format error samtools view: failed to open "1_ucheck.bam" for reading: Exec format error I am not sure about this error. Because from the same fastq file (sample 1), could also align with reference sequence and convert it into a bam file. Websamtools index: failed to create index for "case6.normal.1.bam": No such file or directory My understanding is that samtools index fails if all the reads with no coordinates are NOT …
Samtools index: failed to create index for
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WebDec 24, 2024 · samtools index: failed to create index for merged.sorted.bam": Numerical result out of range" But the human genome does not have that long chromosome. Here is … WebJan 31, 2024 · samtools index: failed to create index for "chr_unplaced.sort.bam": No such file or directory And then I checked the part2.bam, there existed the reads map to the …
http://quinlanlab.org/tutorials/samtools/samtools.html WebSep 27, 2024 · Try using a csi index with min_shift = 14, n_lvls >= 6 samtools index: failed to create index for "18425.bam": Numerical result out of range I rerun mapping using a samtools option samtools...
WebFeb 23, 2024 · samtools index error 0 2.1 years ago pt.taklifi 60 Hello everyone I am trying to extract uniquely aligned reads and sort them with samtools with the following command samtools view -h -f 2 -q 10 -bS -@ 20 hg38.sam samtools sort -n -@ 1 > hg38.sort.bam after this when I try to index the output file samtools index hg38.sort.bam Websamtools idxstats [Data is aligned to hg19 transcriptome]. To use that command I need a sorted bam file. So to sort them I gave the following command. samtools sort -T /tmp/input.sorted -o input.sorted.bam input.bam This ended up showing: [W::bam_hdr_read] EOF marker is absent. The input is probably truncated.
http://quinlanlab.org/tutorials/samtools/samtools.html
WebIndex 64 Rsamtools-package ’samtools’ aligned sequence utilities interface Description This package provides facilities for parsing samtools BAM (binary) files representing aligned se- ... Use BamFile()to create a reference to a BAM file (and optionally its index). The reference remains open across calls to methods, avoiding costly index ... theaters in sacramento areaWebDESCRIPTION Index reference sequence in the FASTA format or extract subsequence from indexed reference sequence. If no region is specified, faidx will index the file and create … the good dish tv today recipesWebApr 14, 2024 · assistant_reply = create_chat_completion(File “C:\AI\AutoGPT\Auto-GPT\scripts\llm_utils.py”, line 50, in create_chat_completion raise RuntimeError(“Failed to … the good dish tv show last episodeWebJul 25, 2024 · 1 Answer. Sorted by: 0. The problem was that although an index must have been build, in the following code instead of passing the index, bcftools mpileup -Ou -f index.fna.fai -b bam_list.txt > raw.bcf. the reference genome must be passed. bcftools mpileup -Ou -f reference.fna -b bam_list.txt > raw.bcf. Share. theaters in rotterdamWebCreate a BAI index. This is currently the default when no format options are used. Create a CSI index. By default, the minimum interval size for the index is 2^14, which is the same … theaters in saginaw mihttp://www.htslib.org/doc/samtools-index.html the good dish websiteWeb© 2024 Slashdot Media. All Rights Reserved. Terms Privacy Opt Out Advertise. Oh no! Some styles failed to load. 😵 Please try reloading this page theaters in rome italy