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Comment: C: awk and sed in bash script and no output
6.9 years ago by WouterDeCoster 48k
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3.9k
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Comment: C: awk and sed in bash script and no output
6.9 years ago by WouterDeCoster 48k
0
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3.9k
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Comment: C: awk and sed in bash script and no output
6.9 years ago by WouterDeCoster 48k
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2
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3.9k
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Comment: C: awk and sed in bash script and no output
6.9 years ago by WouterDeCoster 48k
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1
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3.9k
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Comment: C: Error in prepDE.py in Tuxedo protocol after StringTie quantification
6.9 years ago by WouterDeCoster 48k
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1.5k
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Comment: C: Accessing DEG files with extension dat, phr pin,psq
6.9 years ago by WouterDeCoster 48k
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2
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3.0k
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Answer: A: May I use numreads for doing DGE after quantifying by Salmon
6.9 years ago by WouterDeCoster 48k
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3.0k
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Comment: C: How to extract the same mapped region by multiple samples ?
6.9 years ago by WouterDeCoster 48k
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1.6k
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Comment: C: Criteria for Overlapping SNPs
6.9 years ago by WouterDeCoster 48k
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1
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1.6k
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Answer: A: Criteria for Overlapping SNPs
6.9 years ago by WouterDeCoster 48k
18
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16
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7.1k
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6 follow
Tool to fix reference allele nucleotide in vcf
vcf fasta pony
updated 6.9 years ago by 16k • written 6.9 years ago by 48k
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1
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1.3k
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Comment: C: differently expressed genes
6.9 years ago by WouterDeCoster 48k
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1
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11k
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Comment: C: Remove adaptaters from ONT reads : An alternative to Porechop ?
6.9 years ago by WouterDeCoster 48k
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4.3k
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Answer: A: Demultiplexing before merging paired-end reads?
6.9 years ago by WouterDeCoster 48k
0
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1
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11k
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Comment: C: Remove adaptaters from ONT reads : An alternative to Porechop ?
6.9 years ago by WouterDeCoster 48k
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2.2k
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Comment: C: Take out One percent of the tops of numbers from the column in the table
6.9 years ago by WouterDeCoster 48k
4
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1
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11k
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Answer: A: Remove adaptaters from ONT reads : An alternative to Porechop ?
6.9 years ago by WouterDeCoster 48k
2
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2.3k
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Comment: C: Reasons to refuse to give support
6.9 years ago by WouterDeCoster 48k
3
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3.3k
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Answer: A: structural variant vcf file comparison
6.9 years ago by WouterDeCoster 48k
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1
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4.7k
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Comment: C: How to split BAM files by samples from PacBio
6.9 years ago by WouterDeCoster 48k
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5.7k
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Comment: C: How to identify which SNPs in my dataset are genome wide significant
6.9 years ago by WouterDeCoster 48k
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1.4k
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Comment: C: right genomic coordinate of each gene
6.9 years ago by WouterDeCoster 48k
2
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1
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1.4k
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Comment: C: right genomic coordinate of each gene
6.9 years ago by WouterDeCoster 48k
4
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948
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Answer: A: The order of part processions of RNA-Seq data
6.9 years ago by WouterDeCoster 48k
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3.7k
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Comment: C: VEP output and stop gain mutation
6.9 years ago by WouterDeCoster 48k
0
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0
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3.0k
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Comment: C: How to extract the same mapped region by multiple samples ?
6.9 years ago by WouterDeCoster 48k
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0
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962
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Comment: C: RNA-seq for individual transcripts
6.9 years ago by WouterDeCoster 48k
1
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1
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2.9k
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Comment: C: RNA seq - TMM values
6.9 years ago by WouterDeCoster 48k
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1
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3.7k
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Answer: A: VEP output and stop gain mutation
6.9 years ago by WouterDeCoster 48k
1
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1
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2.9k
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Comment: C: RNA seq - TMM values
6.9 years ago by WouterDeCoster 48k
3
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1
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962
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Answer: C: RNA-seq for individual transcripts
6.9 years ago by WouterDeCoster 48k
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967
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Answer: A: Primer Design for amplifying complete viral genome
6.9 years ago by WouterDeCoster 48k
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1.7k
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Comment: C: Help with whole genome alignment
6.9 years ago by WouterDeCoster 48k
4
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0
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2.9k
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Comment: C: feature extraction from SNPs in R
6.9 years ago by WouterDeCoster 48k
0
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1
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2.9k
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Comment: C: feature extraction from SNPs in R
6.9 years ago by WouterDeCoster 48k
0
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3.4k
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Comment: C: Implement ensembl gene annotation pipeline for my assembly
6.9 years ago by WouterDeCoster 48k
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1
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2.9k
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Comment: C: feature extraction from SNPs in R
6.9 years ago by WouterDeCoster 48k
0
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1
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2.9k
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Comment: C: feature extraction from SNPs in R
6.9 years ago by WouterDeCoster 48k
1
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1
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3.4k
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Comment: C: How can implement ensembl gene annotation pipeline for my data?
6.9 years ago by WouterDeCoster 48k
0
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1
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4.7k
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Comment: C: Using snakemake with multiple output for calling SNP using clairvoyante
6.9 years ago by WouterDeCoster 48k
1
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1
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4.7k
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Answer: A: Using snakemake with multiple output for calling SNP using clairvoyante
6.9 years ago by WouterDeCoster 48k
0
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0
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5.4k
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Comment: C: How to load BAM files that do not have chromosome name in the header?
6.9 years ago by WouterDeCoster 48k
1
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1
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2.2k
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Comment: C: Parsing AME tsv file
6.9 years ago by WouterDeCoster 48k
2
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2
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2.1k
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Comment: C: How would you trim this RNA-seq data
6.9 years ago by WouterDeCoster 48k
1
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0
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1.2k
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Comment: C: What is CINWntUp and CINnormL?
6.9 years ago by WouterDeCoster 48k
0
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0
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3.8k
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Comment: C: Bash: salmon command not found
6.9 years ago by WouterDeCoster 48k
0
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0
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4.4k
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Comment: C: limitations of Edge R or DEseq
6.9 years ago by WouterDeCoster 48k
3
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1
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4.4k
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Comment: C: limitations of Edge R or DEseq
6.9 years ago by WouterDeCoster 48k
0
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1
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1.2k
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Comment: C: What is CINWntUp and CINnormL?
6.9 years ago by WouterDeCoster 48k
0
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1
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2.0k
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Comment: C: gnomAD and Bravo to download loss-of-function annotation
6.9 years ago by WouterDeCoster 48k
7,263 results • Page 29 of 146
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