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Comment: Comment: whatsHap didn't phase all variants
4.4 years ago by WouterDeCoster 48k
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3.5k
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Comment: Comment: What are the columns from pysam fetch?
4.4 years ago by WouterDeCoster 48k
1
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1.8k
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Comment: Comment: VCF filtering
4.4 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Answer: Answer: How to do a pairwise alignment and convert the result to a VCF file?
4.4 years ago by WouterDeCoster 48k
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2.6k
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Comment: Comment: reference fasta creation
4.4 years ago by WouterDeCoster 48k
2
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598
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Comment: Comment: Compatilibity between human37 and human38 gtf
4.4 years ago by WouterDeCoster 48k
1
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2.3k
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Comment: Comment: Variable numbers of Reads. I'm lost
4.4 years ago by WouterDeCoster 48k
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1.2k
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Comment: Comment: Does GISAID fasta files contain spike protein or whole genome sequence?
4.4 years ago by WouterDeCoster 48k
1
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1
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1.4k
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Answer: Answer: Why we have exons that start and end at the same coordinate?!
4.4 years ago by WouterDeCoster 48k
0
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2.0k
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Comment: Comment: Remove reads from bam file that partially covers a region
4.4 years ago by WouterDeCoster 48k
1
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1
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1.9k
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Comment: Comment: Where to get consensus sequences of human transposable elements
4.4 years ago by WouterDeCoster 48k
0
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1.9k
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Comment: Comment: Where to get consensus sequences of human transposable elements
4.4 years ago by WouterDeCoster 48k
4
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4
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1.9k
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Where to get consensus sequences of human transposable elements
database transposons reference
updated 4.4 years ago by 5.3k • written 4.4 years ago by 48k
2
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0
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2.3k
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Answer: Answer: merge .fastq.gz files
4.5 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: Workflow for structural variants from long read sequencing data
4.5 years ago by WouterDeCoster 48k
1
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1
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1.4k
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Answer: A: preprocess of the nanopore seqeucning data
4.5 years ago by WouterDeCoster 48k
0
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0
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958
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Comment: C: how to check significant differential methylation, hypermethylated or hypomethyl
4.5 years ago by WouterDeCoster 48k
0
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0
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953
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Comment: C: How to create a genome assembler?
4.5 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: Estimate running time of a program
4.5 years ago by WouterDeCoster 48k
0
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1
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977
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Comment: C: get coordinates for a list of genes
4.5 years ago by WouterDeCoster 48k
0
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1.7k
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Comment: C: What are some areas of bioinformatics that are overdone?
4.6 years ago by WouterDeCoster 48k
2
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0
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12k
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Comment: C: BAM to FASTQ picard or samtools
4.6 years ago by WouterDeCoster 48k
0
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1
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1.6k
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Comment: C: Analysis of genotype g.vcf
4.6 years ago by WouterDeCoster 48k
0
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1
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1.4k
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Comment: C: development of NGS pipeline for variant calling in lung cancer
4.6 years ago by WouterDeCoster 48k
0
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1
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1.6k
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Comment: C: Analysis of genotype g.vcf
4.6 years ago by WouterDeCoster 48k
0
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1
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1.0k
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Comment: C: system commands from R containing single and double quotes
4.6 years ago by WouterDeCoster 48k
0
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1
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6.3k
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Comment: C: bcftools filter or bcftools isec to EXCLUDE dbSNP snps
4.6 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: WGCNA: very low genes assigned to the grey Module
4.6 years ago by WouterDeCoster 48k
4
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1
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2.4k
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Answer: A: Where to start? Newbie trying to enter the world of computational biology gettin
4.7 years ago by WouterDeCoster 48k
0
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1
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1.4k
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Comment: C: Papers/posts on best practises for dealing with Illumina reads?
4.7 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: Adding read group (@RG) information when there are multiple ID's.
4.7 years ago by WouterDeCoster 48k
0
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0
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4.1k
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Comment: C: Which adapters to use for trimming?
4.7 years ago by WouterDeCoster 48k
0
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0
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2.7k
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Comment: C: Can you tell whether the cell was dead or not using RNA-seq data?
4.7 years ago by WouterDeCoster 48k
0
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0
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1.1k
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Comment: C: How to check size of genome?
4.7 years ago by WouterDeCoster 48k
0
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0
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1.1k
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Comment: C: How to get independent loci from gwas variants
4.7 years ago by WouterDeCoster 48k
0
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1
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1.1k
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Comment: C: How to get independent loci from gwas variants
4.7 years ago by WouterDeCoster 48k
0
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1
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1.1k
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Comment: C: How to get independent loci from gwas variants
4.7 years ago by WouterDeCoster 48k
1
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0
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3.7k
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Comment: C: Demultiplexing MinION reads with Illumina barcodes/adapters?
4.7 years ago by WouterDeCoster 48k
0
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1
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1.0k
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Comment: C: help me to r
4.7 years ago by WouterDeCoster 48k
2
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1
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2.2k
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Answer: A: Adding read group (@RG) information when there are multiple ID's.
4.7 years ago by WouterDeCoster 48k
2
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0
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4.2k
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Answer: C: BWA mem for many RNA.seq reads align to reference
4.7 years ago by WouterDeCoster 48k
2
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0
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1.0k
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Answer: A: Does HTSEQ output include non-coding genes also?
4.8 years ago by WouterDeCoster 48k
0
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0
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1.6k
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Comment: C: Knowing the number of exons in a range
4.8 years ago by WouterDeCoster 48k
0
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1
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1.6k
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Comment: C: Knowing the number of exons in a range
4.8 years ago by WouterDeCoster 48k
2
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1
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5.4k
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Comment: C: Best ubuntu version for bioinformatics?
4.8 years ago by WouterDeCoster 48k
0
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1
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3.7k
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Comment: C: Extracting Methylation Data
4.8 years ago by WouterDeCoster 48k
2
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0
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3.0k
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Comment: C: How to run R script in linux system
4.8 years ago by WouterDeCoster 48k
0
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0
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1.3k
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Comment: C: SNP index definition
4.8 years ago by WouterDeCoster 48k
0
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0
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1.9k
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Comment: C: Counting data with ht seq
4.8 years ago by WouterDeCoster 48k
0
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0
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3.9k
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Comment: C: why the p-value is 0?
4.8 years ago by WouterDeCoster 48k
7,263 results • Page 4 of 146
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