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Comment: Filtered reads from assembly and raw reads?
Comment: Multi-allelic sites in Identity-by-descent tract detection
A: How to find the mean inter-marker distance between SNPs from a vcf file?
Comment: resolving specific clusters from data (spectral clustering)
Answer: How to split a long protein sequence in small sequences with same header?
Answer: How to split a long protein sequence in small sequences with same header?
Answer: How to split a long protein sequence in small sequences with same header?
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Comment: Finding the read ratio of transcription termination data using R
by
margo
▴ 20
Thank you for getting back to me. I have converted my bedgraph file to a dataframe. I am wanting to write a code which applies the function…
Answer: Supplementary alignments in BAM-file
by
Carlo Yague
8.1k
In one step, you could remove every alignments with a mapping quality of 0. With most aligners, this corresponds to the reads for which the…
Answer: Finding the read ratio of transcription termination data using R
by
Trivas
▴ 420
Please do not use bedgraph files for this type of analysis. I've used bed files and `bedtools coverage` to calculate the coverage within sp…
Comment: BWA-mem - Different alignment numbers to same reference sequence
by
GenoMax
117k
Likely since OP says > small sequences of around 150bp
Comment: BWA-mem - Different alignment numbers to same reference sequence
by
GenoMax
117k
May be of interest: https://jeremy9959.net/Blog/TheMEMinBWAMem-fixed/
Answer: Supplementary alignments in BAM-file
by
swbarnes2
12k
It might take two steps: 1) using samtools to identify the read names which have supplementary alignments, then 2) filter away all lines in…
Comment: BWA-mem - Different alignment numbers to same reference sequence
by
swbarnes2
12k
Are those 75k reads longer than seq2?
Comment: How to split a long protein sequence in small sequences with same header?
by
shenwei356
7.3k
seqkit does not work on this case.
Comment: How to split a long protein sequence in small sequences with same header?
by
cpad0112
21k
if fasta file is as simple as that, you can try following simple code: $ bioawk -c fastx '{print ">"$name; print substr($seq,1,length(…
Comment: Supplementary alignments in BAM-file
by
GenoMax
117k
Does this address > i want the whole read to be filtered out whenever it contains > supplementary alignments from the bamfile and not on…
Answer: Supplementary alignments in BAM-file
by
Pierre Lindenbaum
146k
add `-e '![SA]'` to your samtools view command ( http://www.htslib.org/doc/samtools.html#FILTER_EXPRESSIONS )
Comment: Minimum and maximum depth filert - vcftools
by
Pierre Lindenbaum
146k
vcftools is deprecated use `bcftools -i 'INFODP>1 && INFO/DP<1000'`
Comment: Filtered reads from assembly and raw reads?
by
GenoMax
117k
> can be used to get reads from a de-novo assembly if I have the raw > reads? If you have an assembly then the individual reads are no lon…
Answer: ESTIMATION OF LEVEL OF CYTOKINES FROM BULK RNAseq
by
Rafael Soler
▴ 430
Hello Leticia, I don't know much about Cybersort analysis, but you can check genes related to `cytokine activity` GO Term http://www.inf…
Comment: Supplementary alignments in BAM-file
by
mokbel73
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