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Comment: Comment: all coding regions .bed file hg38 Whole Genome Sequencing
6 weeks ago by Dataman ▴ 350
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2.8k
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Comment: Comment: Did anyone success in working with the broad ABSOLUTE?
7 weeks ago by Dataman ▴ 350
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0
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12k
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Comment: Comment: Anyone Has A Working Example On How To Run BROAD's ABSOLUTE On Exome Sequencing
7 weeks ago by Dataman ▴ 350
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1
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325
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Comment: Comment: What are accession numbers starting with PIR e.g. PIR60289?
5 months ago by Dataman ▴ 350
3
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3
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325
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What are accession numbers starting with PIR e.g. PIR60289?
accession_number
updated 5 months ago by 14k • written 5 months ago by ▴ 350
0
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2.2k
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Comment: Comment: GATK4 ASEReadCounter returns nothing
6 months ago by Dataman ▴ 350
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0
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9.2k
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Comment: Comment: Fisher'S Exact Test And Odds Ratio
6 months ago by Dataman ▴ 350
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5.1k
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Comment: Comment: What is allele-specific binding, allele-specific expression, and allelic imbalan
7 months ago by Dataman ▴ 350
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1
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5.8k
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Comment: C: ChIP seq basic terminology: what is a ChIP-seq tag?
updated 2.0 years ago by 93k • written 2.0 years ago by ▴ 350
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0
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7.1k
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Comment: C: Convert Tab delimited file to VCF file
2.4 years ago by Dataman ▴ 350
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0
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22k
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Comment: Comment: SNP annotation tool
updated 5 months ago by 36k • written 2.5 years ago by ▴ 350
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0
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1.1k
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Comment: C: GATK HaplotypeCaller/GenotypeGVCFs assigning GQ 0 and GT ./. at well-covered, hi
2.5 years ago by Dataman ▴ 350
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0
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4.2k
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Comment: C: How to create B-allele frequency file for ADTEx?
updated 2.5 years ago by 36k • written 6.4 years ago by ▴ 350
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1
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7.7k
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Comment: C: DP in VCF files?
2.5 years ago by Dataman ▴ 350
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1
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7.7k
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Comment: C: DP in VCF files?
2.5 years ago by Dataman ▴ 350
0
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0
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5.0k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
updated 2.5 years ago by 36k • written 6.5 years ago by ▴ 350
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0
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5.0k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
updated 2.5 years ago by 36k • written 6.5 years ago by ▴ 350
0
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1
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3.9k
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Comment: C: Removing the OQ tag from a BAM file
updated 2.5 years ago by 36k • written 6.5 years ago by ▴ 350
0
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0
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5.0k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
updated 2.5 years ago by 36k • written 6.5 years ago by ▴ 350
1
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0
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18k
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Answer: A: Recommendations For Python Vcf Parser/Writer?
2.7 years ago by Dataman ▴ 350
0
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1
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2.7k
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Answer: A: How to create a pooled normal exome sample?
updated 2.7 years ago by 36k • written 7.0 years ago by ▴ 350
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0
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22k
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Comment: C: What is the difference between narrow peak, Broad peak and a gapped peak of a c
2.8 years ago by Dataman ▴ 350
2
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0
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29k
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Comment: C: ATAC-seq peak calling with MACS
2.8 years ago by Dataman ▴ 350
0
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0
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13k
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Comment: C: How To Count The Reads Mapped To Exon And Exon-Exon Junctions?
2.8 years ago by Dataman ▴ 350
1
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1
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5.0k
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Comment: C: vcfanno quickly annotate a vcf with other VCFs, BEDs, BAMs
2.8 years ago by Dataman ▴ 350
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0
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2.9k
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Comment: C: Quality Control Software For Targeted Sequencing?
3.4 years ago by Dataman ▴ 350
0
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0
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2.9k
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Comment: C: Quality Control Software For Targeted Sequencing?
3.4 years ago by Dataman ▴ 350
3
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5
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1.7k
views
What kind of systematic bias of sequencing data the following normalization procedure address?
next-gen normalization bias
updated 3.8 years ago by 36k • written 6.4 years ago by ▴ 350
0
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1
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1.7k
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Comment: C: What kind of systematic bias of sequencing data the following normalization proc
updated 3.8 years ago by 36k • written 6.4 years ago by ▴ 350
0
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0
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1.7k
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Comment: C: What kind of systematic bias of sequencing data the following normalization proc
updated 3.8 years ago by 36k • written 6.4 years ago by ▴ 350
28
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9
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22k
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samtools bedcov vs. bedtools coverage
DNA-seq coverage
updated 3.8 years ago by 36k • written 6.1 years ago by ▴ 350
0
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0
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26k
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Comment: C: What Makes One Probability Distribution Better For Rna-Seq Than Another?
4.1 years ago by Dataman ▴ 350
0
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0
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4.0k
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Comment: C: Why Is Snp Data Generally Restricted?
4.5 years ago by Dataman ▴ 350
0
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1
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153k
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Comment: C: Forward And Reverse Strand Conventions
4.6 years ago by Dataman ▴ 350
0
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0
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3.7k
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Comment: C: demultiplexing Illumina output with fastq_multx
4.7 years ago by Dataman ▴ 350
0
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1
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3.7k
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Comment: C: demultiplexing Illumina output with fastq_multx
4.7 years ago by Dataman ▴ 350
20
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16
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4.6k
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Breaking down the reference genome chromosome-wise
reference_genome fasta
updated 5 months ago by 36k • written 7.7 years ago by ▴ 350
0
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3
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2.7k
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How to create a pooled normal exome sample?
next-gen sequencing exome copy number analysis
updated 4.8 years ago by ▴ 180 • written 7.0 years ago by ▴ 350
0
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0
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8.7k
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Comment: C: Calculating GC content from BAM file by BED file
5.2 years ago by Dataman ▴ 350
0
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1
reply
19k
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Comment: C: Bioinformatics courses, workshops or training
5.2 years ago by Dataman ▴ 350
0
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2
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19k
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Comment: C: Bioinformatics courses, workshops or training
5.2 years ago by Dataman ▴ 350
1
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0
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45k
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Comment: C: Subsampling Bam File With Samtools
5.4 years ago by Dataman ▴ 350
1
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0
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54k
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Comment: C: What is difference between soft-clipped and hard-clipped in SAM specification?
5.5 years ago by Dataman ▴ 350
0
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0
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47k
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Comment: C: How To Sort Bed Format File
5.8 years ago by Dataman ▴ 350
0
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1
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14k
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Comment: C: How To Compute Gene Enrichment P-Value? (Significantly More Than Expected)
5.9 years ago by Dataman ▴ 350
1
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0
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1.4k
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Answer: A: Is there mirwalk2.0 client-side or library?
5.9 years ago by Dataman ▴ 350
2
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1
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2.4k
views
Answer: A: What training do you think a computer scientist should do to move into the bioin
5.9 years ago by Dataman ▴ 350
0
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0
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1.8k
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Best way to normalize Human BodyMap 2.0 data
RNA-Seq normalization
updated 5.9 years ago by 20 • written 6.7 years ago by ▴ 350
1
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0
replies
25k
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Comment: C: Extracting List Of Genes Associated With A Pathway In Kegg
6.0 years ago by Dataman ▴ 350
0
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0
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1.1k
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Comment: C: rename Fasta file headings for use in MIRA
6.0 years ago by Dataman ▴ 350
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