Bismark
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A tool to map bisulfite converted sequence reads and determine cytosine methylation states
  The data I used was processed by fastqc and Trim_galore. And it is processed by bismark, deduplicate_bismark and bismark_methylation_extractor as specified in the manual. As can be seen...
Hello there I am running into an issue while running the human genome on the test file below. After I do the genome prep I see these messages. I verified...
Hi Team, I am running Bismark with the below command. I can see it's really slow. bismark --bowtie2 -N 1 --parallel 4 $RESOURCES2/HG38/ -1 $Read1 -2 $Read2 --output_dir $PWD --temp_dir...
Hello, I have some DNA methylation data, which I prepared using EM-Seq and got around 236 million paired-end reads after sequencing on the Illumina NextSeq platform. I have some concerns...
I have read many closed issues with a similar problem: #211 #219 #360 I used the module already set up in the supercomputer (ver. 0.24.1). Here is one of the...
Hi Felix, I am sorry to trouble you. I’m having some trouble with the FastQC report and would like to ask you. 1. According to the “Per base sequence content”,...
This is not really a bug as the documentation clearly states how deduplicate_bismark expects UMIs to be handled, but it is an easy mistake to make. As documented in deduplicate_bismark,...
Dear Felix, Thank you so much for developing this great tool! I rely Bismark heavily for my research :) Recently we developed a haplotype-resolved diploid human genome, where one copy...
bismark  the map command : /bismark --genome_folder ../01.hap1 --hisat2 --non_directional -1 ../clean_ZHM1H.R1.fastq.gz -2 ../clean_ZHM1H.R2.fastq.gz -p 5 -L 30 -N 1 -o hap1 #--output_dir ./ --bam hap1_bismark_hisat2_pe.bam my friends, what's...
Hello I had trouble with uploading my read files in a sever to do Bismark analysis cause they are so big (about 20 G). I compressed them with winRar and...