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Comment: Comment: How to search for genes 100Kb up and downstream of any genomic site
2.9 years ago by WouterDeCoster 47k
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627
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Comment: Comment: What tools are best for conjoined gene/readthough detection and how do they diff
2.9 years ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: FeatureCounts Number of Reads
2.9 years ago by WouterDeCoster 47k
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15k
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Comment: Comment: How to trim Nanopore reads. Please suggest a tool.
2.9 years ago by WouterDeCoster 47k
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832
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Comment: Comment: whole tissue and RNA-seq: can I still study specific cell types?
3.0 years ago by WouterDeCoster 47k
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832
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Comment: Comment: whole tissue and RNA-seq: can I still study specific cell types?
3.0 years ago by WouterDeCoster 47k
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1.7k
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Comment: Comment: Hello everyone whenever i run this command this error terminates the command. ca
3.0 years ago by WouterDeCoster 47k
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1.7k
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Comment: Comment: Hello everyone whenever i run this command this error terminates the command. ca
3.0 years ago by WouterDeCoster 47k
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1
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3.5k
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Comment: Comment: How to install argparse for python 2.7
3.0 years ago by WouterDeCoster 47k
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10k
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Comment: Comment: Change header of a Fasta file according to the file name
3.0 years ago by WouterDeCoster 47k
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2.5k
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Comment: Comment: How to interpret a FASTA file
3.0 years ago by WouterDeCoster 47k
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2.5k
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Comment: Comment: How to interpret a FASTA file
updated 3.0 years ago by 15k • written 3.0 years ago by 47k
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3.2k
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Comment: Comment: Trimming on Nanopore Data
3.0 years ago by WouterDeCoster 47k
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753
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Comment: Comment: How to use python to align 30 kb genome to another 30kb reference, repeat 10x ti
3.0 years ago by WouterDeCoster 47k
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1.5k
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Comment: Comment: whatsHap didn't phase all variants
3.0 years ago by WouterDeCoster 47k
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2.6k
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Comment: Comment: What are the columns from pysam fetch?
3.0 years ago by WouterDeCoster 47k
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1.3k
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Comment: Comment: VCF filtering
3.0 years ago by WouterDeCoster 47k
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1.7k
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Comment: Comment: reference fasta creation
3.0 years ago by WouterDeCoster 47k
2
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405
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Comment: Comment: Compatilibity between human37 and human38 gtf
3.0 years ago by WouterDeCoster 47k
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1.4k
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Comment: Comment: Variable numbers of Reads. I'm lost
3.1 years ago by WouterDeCoster 47k
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813
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Comment: Comment: Does GISAID fasta files contain spike protein or whole genome sequence?
3.1 years ago by WouterDeCoster 47k
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1.5k
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Comment: Comment: Remove reads from bam file that partially covers a region
3.1 years ago by WouterDeCoster 47k
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1
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1.3k
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Comment: Comment: Where to get consensus sequences of human transposable elements
3.1 years ago by WouterDeCoster 47k
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1.3k
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Comment: Comment: Where to get consensus sequences of human transposable elements
3.1 years ago by WouterDeCoster 47k
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2.5k
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Comment: C: Workflow for structural variants from long read sequencing data
3.2 years ago by WouterDeCoster 47k
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792
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Comment: C: how to check significant differential methylation, hypermethylated or hypomethyl
3.2 years ago by WouterDeCoster 47k
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634
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Comment: C: How to create a genome assembler?
3.2 years ago by WouterDeCoster 47k
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1.3k
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Comment: C: Estimate running time of a program
3.2 years ago by WouterDeCoster 47k
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1
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682
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Comment: C: get coordinates for a list of genes
3.2 years ago by WouterDeCoster 47k
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1.1k
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Comment: C: What are some areas of bioinformatics that are overdone?
3.2 years ago by WouterDeCoster 47k
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10k
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Comment: C: BAM to FASTQ picard or samtools
3.2 years ago by WouterDeCoster 47k
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1
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1.2k
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Comment: C: Analysis of genotype g.vcf
3.3 years ago by WouterDeCoster 47k
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1
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898
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Comment: C: development of NGS pipeline for variant calling in lung cancer
3.3 years ago by WouterDeCoster 47k
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1
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1.2k
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Comment: C: Analysis of genotype g.vcf
3.3 years ago by WouterDeCoster 47k
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1
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736
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Comment: C: system commands from R containing single and double quotes
3.3 years ago by WouterDeCoster 47k
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1
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5.3k
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Comment: C: bcftools filter or bcftools isec to EXCLUDE dbSNP snps
3.3 years ago by WouterDeCoster 47k
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1
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1.6k
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Comment: C: WGCNA: very low genes assigned to the grey Module
3.3 years ago by WouterDeCoster 47k
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1
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924
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Comment: C: Papers/posts on best practises for dealing with Illumina reads?
3.3 years ago by WouterDeCoster 47k
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1.5k
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Comment: C: Adding read group (@RG) information when there are multiple ID's.
3.3 years ago by WouterDeCoster 47k
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2.9k
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Comment: C: Which adapters to use for trimming?
3.3 years ago by WouterDeCoster 47k
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1.9k
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Comment: C: Can you tell whether the cell was dead or not using RNA-seq data?
3.3 years ago by WouterDeCoster 47k
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681
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Comment: C: How to check size of genome?
3.3 years ago by WouterDeCoster 47k
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761
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Comment: C: How to get independent loci from gwas variants
3.3 years ago by WouterDeCoster 47k
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1
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761
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Comment: C: How to get independent loci from gwas variants
3.3 years ago by WouterDeCoster 47k
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1
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761
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Comment: C: How to get independent loci from gwas variants
3.3 years ago by WouterDeCoster 47k
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2.7k
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Comment: C: Demultiplexing MinION reads with Illumina barcodes/adapters?
3.4 years ago by WouterDeCoster 47k
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1
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743
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Comment: C: help me to r
3.4 years ago by WouterDeCoster 47k
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954
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Comment: C: Knowing the number of exons in a range
3.4 years ago by WouterDeCoster 47k
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1
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954
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Comment: C: Knowing the number of exons in a range
3.4 years ago by WouterDeCoster 47k
2
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1
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3.4k
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Comment: C: Best ubuntu version for bioinformatics?
3.4 years ago by WouterDeCoster 47k
6,245 results • Page 3 of 125
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