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Comment: C: Test for recombination in a clonal tetraploid?
updated 5.8 years ago by 45k • written 11.4 years ago by ★ 4.3k
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0
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5.9k
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Comment: C: Looking For Phd Program Focus On Genomics
updated 5.9 years ago by 45k • written 13.7 years ago by ★ 4.3k
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7.0k
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Comment: C: Tf-Target Enrichment Analysis
updated 5.9 years ago by 45k • written 14.1 years ago by ★ 4.3k
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0
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5.9k
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Comment: C: What Features From Publishers Would Help Bioinformatics Folks?
updated 5.9 years ago by 45k • written 14.3 years ago by ★ 4.3k
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20k
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Comment: C: How To Combine Two Samtools Commands.
updated 6.1 years ago by 45k • written 13.5 years ago by ★ 4.3k
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5.3k
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Comment: C: NOT RESETTING NORMAL error using Varscan2
updated 6.1 years ago by 45k • written 10.9 years ago by ★ 4.3k
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3.6k
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Comment: C: Crlmm Package And Genotyping With Snp 5 Chips (Affy)
updated 6.1 years ago by 45k • written 13.6 years ago by ★ 4.3k
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0
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7.3k
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Comment: C: Conversion Of Grangeslist To Gff File
updated 6.1 years ago by 45k • written 13.6 years ago by ★ 4.3k
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0
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8.8k
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Comment: C: Generating Mappability Files
updated 6.1 years ago by 45k • written 13.6 years ago by ★ 4.3k
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0
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11k
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Comment: C: How To Differentiate Between Mate Pair And Paired End Reads Based On Sam Flag
updated 6.1 years ago by 45k • written 14.2 years ago by ★ 4.3k
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0
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12k
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Comment: C: What Is Best Current Dna Compression Algorithm?
updated 6.1 years ago by 45k • written 13.9 years ago by ★ 4.3k
1
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0
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27k
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Comment: C: Bioinformatics "Cheat Sheet"
updated 6.2 years ago by 45k • written 14.2 years ago by ★ 4.3k
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0
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4.3k
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Comment: C: Batch correction for TCGA 450K data
9.7 years ago by Ying W ★ 4.3k
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0
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4.6k
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Comment: C: RUVseq to correct for unwanted variance, interpreting p-value distribution
9.9 years ago by Ying W ★ 4.3k
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1
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4.6k
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Comment: C: RUVseq to correct for unwanted variance, interpreting p-value distribution
10.0 years ago by Ying W ★ 4.3k
0
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1
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7.7k
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Comment: C: Do specialized Hi-C databases exist?
10.2 years ago by Ying W ★ 4.3k
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0
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8.4k
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Comment: C: Annotating Chip Seq: How To Get Enrichment Over Random Background
10.2 years ago by Ying W ★ 4.3k
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0
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9.5k
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Comment: Comment: TCGA: How to tell if the data is exome or WGS?
updated 3.1 years ago by 45k • written 10.2 years ago by ★ 4.3k
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0
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4.2k
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Comment: Comment: Issues with DiffBind
updated 3.1 years ago by 45k • written 10.2 years ago by ★ 4.3k
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0
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5.8k
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Comment: C: What criteria are used to determine supplementary alignment with bwa-mem (flag 2
10.3 years ago by Ying W ★ 4.3k
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1
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2.6k
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Comment: Comment: ChIPQC showed errors 'nnodes' must be >= 1
updated 3.1 years ago by 45k • written 10.3 years ago by ★ 4.3k
2
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1
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21k
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Comment: Comment: Limma package: explanation makeContrasts examples
updated 3.1 years ago by 45k • written 10.3 years ago by ★ 4.3k
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0
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3.6k
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Comment: C: Is there any differnce between using biomaRt package under R to retrieve gene in
10.4 years ago by Ying W ★ 4.3k
0
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1
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3.6k
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Comment: C: Is there any differnce between using biomaRt package under R to retrieve gene in
10.4 years ago by Ying W ★ 4.3k
0
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0
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8.5k
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Comment: C: Tumor clonality algorithms
10.4 years ago by Ying W ★ 4.3k
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0
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4.2k
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Comment: C: How to produce a hom/het snp frequency table
10.4 years ago by Ying W ★ 4.3k
0
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0
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8.5k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
10.4 years ago by Ying W ★ 4.3k
1
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1
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4.5k
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Comment: C: Named variants to Rsids or coordinates or Haplotype?
10.4 years ago by Ying W ★ 4.3k
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0
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30k
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Comment: C: hg19 vs hg38 in two pictures
10.4 years ago by Ying W ★ 4.3k
1
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0
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6.0k
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Comment: C: Sliding Window for CNV Analysis
10.4 years ago by Ying W ★ 4.3k
2
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2
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8.5k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
10.4 years ago by Ying W ★ 4.3k
0
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0
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8.5k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
10.4 years ago by Ying W ★ 4.3k
0
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1
reply
2.9k
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Comment: C: help: smartpca plot population shift problem
10.4 years ago by Ying W ★ 4.3k
0
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1
reply
4.2k
views
Comment: C: How to produce a hom/het snp frequency table
10.4 years ago by Ying W ★ 4.3k
0
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0
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3.0k
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Comment: C: What is the difference between fine-mapping and targeted sequencing?
10.4 years ago by Ying W ★ 4.3k
0
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1
reply
3.7k
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Comment: Comment: ReadVCF not reading samples
updated 2.8 years ago by 45k • written 10.4 years ago by ★ 4.3k
0
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1
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3.3k
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Comment: Comment: Quality scores in ICGC simple somatic mutation file
updated 2.8 years ago by 45k • written 10.4 years ago by ★ 4.3k
0
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1
reply
11k
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Comment: C: Samtools mpileup quality scores all zero
10.4 years ago by Ying W ★ 4.3k
0
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1
reply
11k
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Comment: C: Samtools mpileup quality scores all zero
10.4 years ago by Ying W ★ 4.3k
3
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1
reply
28k
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Comment: Comment: Bioinformatics courses, workshops or training
updated 2.8 years ago by 45k • written 10.4 years ago by ★ 4.3k
1
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1
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2.4k
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Comment: C: mitochondrial variants in familial disease
10.4 years ago by Ying W ★ 4.3k
1
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0
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4.3k
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Comment: Comment: Cost of computing
updated 2.8 years ago by 45k • written 10.4 years ago by ★ 4.3k
1
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1
reply
11k
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Comment: C: Samtools mpileup quality scores all zero
10.4 years ago by Ying W ★ 4.3k
1
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1
reply
4.6k
views
Comment: C: Comparing TMM and RSEM RNASeq data
10.4 years ago by Ying W ★ 4.3k
1
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0
replies
4.3k
views
Comment: Comment: Matching Gencode annotations to Assemblies
updated 2.8 years ago by 45k • written 10.5 years ago by ★ 4.3k
0
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0
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4.6k
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Comment: C: Illumina BeadChip Replicate Probes
10.6 years ago by Ying W ★ 4.3k
0
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0
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8.4k
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Comment: C: Distribution Of Gene Size
10.6 years ago by Ying W ★ 4.3k
1
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1
reply
4.3k
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Comment: C: What is the correct way to use GNU parallel with Primer3?
10.6 years ago by Ying W ★ 4.3k
0
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0
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2.0k
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Comment: C: Unpacking reference file for Isaac Aligner
10.7 years ago by Ying W ★ 4.3k
0
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1
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4.8k
views
Comment: Comment: problems in Diffbind In Creating Diffbind Object In R For Chip-Seq Peaks
updated 3.6 years ago by 45k • written 10.7 years ago by ★ 4.3k
179 results • Page 1 of 4
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