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Comment: C: Test for recombination in a clonal tetraploid?
updated 3.7 years ago by 40k • written 9.3 years ago by ★ 4.2k
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4.1k
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Comment: C: Looking For Phd Program Focus On Genomics
updated 3.8 years ago by 40k • written 11.6 years ago by ★ 4.2k
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Comment: C: Tf-Target Enrichment Analysis
updated 3.8 years ago by 40k • written 12.0 years ago by ★ 4.2k
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0
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3.6k
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Comment: C: What Features From Publishers Would Help Bioinformatics Folks?
updated 3.8 years ago by 40k • written 12.2 years ago by ★ 4.2k
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17k
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Comment: C: How To Combine Two Samtools Commands.
updated 4.0 years ago by 40k • written 11.4 years ago by ★ 4.2k
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4.3k
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Comment: C: NOT RESETTING NORMAL error using Varscan2
updated 4.0 years ago by 40k • written 8.8 years ago by ★ 4.2k
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3.0k
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Comment: C: Crlmm Package And Genotyping With Snp 5 Chips (Affy)
updated 4.0 years ago by 40k • written 11.5 years ago by ★ 4.2k
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0
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6.4k
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Comment: C: Conversion Of Grangeslist To Gff File
updated 4.0 years ago by 40k • written 11.5 years ago by ★ 4.2k
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0
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6.8k
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Comment: C: Generating Mappability Files
updated 4.0 years ago by 40k • written 11.5 years ago by ★ 4.2k
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0
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10.0k
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Comment: C: How To Differentiate Between Mate Pair And Paired End Reads Based On Sam Flag
updated 4.0 years ago by 40k • written 12.1 years ago by ★ 4.2k
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9.8k
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Comment: C: What Is Best Current Dna Compression Algorithm?
updated 4.0 years ago by 40k • written 11.7 years ago by ★ 4.2k
1
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0
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19k
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Comment: C: Bioinformatics "Cheat Sheet"
updated 4.0 years ago by 40k • written 12.1 years ago by ★ 4.2k
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0
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3.6k
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Comment: C: Batch correction for TCGA 450K data
7.6 years ago by Ying W ★ 4.2k
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0
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3.5k
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Comment: C: RUVseq to correct for unwanted variance, interpreting p-value distribution
7.8 years ago by Ying W ★ 4.2k
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1
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3.5k
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Comment: C: RUVseq to correct for unwanted variance, interpreting p-value distribution
7.8 years ago by Ying W ★ 4.2k
0
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1
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5.9k
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Comment: C: Do specialized Hi-C databases exist?
8.1 years ago by Ying W ★ 4.2k
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0
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7.3k
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Comment: C: Annotating Chip Seq: How To Get Enrichment Over Random Background
8.1 years ago by Ying W ★ 4.2k
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0
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7.9k
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Comment: Comment: TCGA: How to tell if the data is exome or WGS?
updated 12 months ago by 40k • written 8.1 years ago by ★ 4.2k
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3.3k
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Comment: Comment: Issues with DiffBind
updated 11 months ago by 40k • written 8.1 years ago by ★ 4.2k
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0
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4.8k
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Comment: C: What criteria are used to determine supplementary alignment with bwa-mem (flag 2
8.1 years ago by Ying W ★ 4.2k
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1
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1.9k
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Comment: Comment: ChIPQC showed errors 'nnodes' must be >= 1
updated 11 months ago by 40k • written 8.1 years ago by ★ 4.2k
2
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1
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16k
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Comment: Comment: Limma package: explanation makeContrasts examples
updated 11 months ago by 40k • written 8.2 years ago by ★ 4.2k
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0
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2.6k
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Comment: C: Is there any differnce between using biomaRt package under R to retrieve gene in
8.3 years ago by Ying W ★ 4.2k
0
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1
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2.6k
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Comment: C: Is there any differnce between using biomaRt package under R to retrieve gene in
8.3 years ago by Ying W ★ 4.2k
0
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0
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6.9k
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Comment: C: Tumor clonality algorithms
8.3 years ago by Ying W ★ 4.2k
0
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0
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2.9k
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Comment: C: How to produce a hom/het snp frequency table
8.3 years ago by Ying W ★ 4.2k
0
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0
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6.0k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
8.3 years ago by Ying W ★ 4.2k
1
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1
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3.0k
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Comment: C: Named variants to Rsids or coordinates or Haplotype?
8.3 years ago by Ying W ★ 4.2k
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0
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27k
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Comment: C: hg19 vs hg38 in two pictures
8.3 years ago by Ying W ★ 4.2k
1
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0
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4.5k
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Comment: C: Sliding Window for CNV Analysis
8.3 years ago by Ying W ★ 4.2k
2
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2
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6.0k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
8.3 years ago by Ying W ★ 4.2k
0
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0
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6.0k
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Comment: C: How to handle chr Y data in BAM files from exome sequencing of human females
8.3 years ago by Ying W ★ 4.2k
0
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1
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2.4k
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Comment: C: help: smartpca plot population shift problem
8.3 years ago by Ying W ★ 4.2k
0
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1
reply
2.9k
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Comment: C: How to produce a hom/het snp frequency table
8.3 years ago by Ying W ★ 4.2k
0
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0
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2.4k
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Comment: C: What is the difference between fine-mapping and targeted sequencing?
8.3 years ago by Ying W ★ 4.2k
0
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1
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2.8k
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Comment: Comment: ReadVCF not reading samples
updated 8 months ago by 40k • written 8.3 years ago by ★ 4.2k
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1
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2.5k
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Comment: Comment: Quality scores in ICGC simple somatic mutation file
updated 8 months ago by 40k • written 8.3 years ago by ★ 4.2k
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1
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8.2k
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Comment: C: Samtools mpileup quality scores all zero
8.3 years ago by Ying W ★ 4.2k
0
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1
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8.2k
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Comment: C: Samtools mpileup quality scores all zero
8.3 years ago by Ying W ★ 4.2k
3
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1
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21k
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Comment: Comment: Bioinformatics courses, workshops or training
updated 8 months ago by 40k • written 8.3 years ago by ★ 4.2k
1
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1
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1.6k
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Comment: C: mitochondrial variants in familial disease
8.3 years ago by Ying W ★ 4.2k
1
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0
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2.4k
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Comment: Comment: Cost of computing
updated 8 months ago by 40k • written 8.3 years ago by ★ 4.2k
1
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1
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8.2k
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Comment: C: Samtools mpileup quality scores all zero
8.3 years ago by Ying W ★ 4.2k
1
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1
reply
3.5k
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Comment: C: Comparing TMM and RSEM RNASeq data
8.3 years ago by Ying W ★ 4.2k
1
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0
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3.2k
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Comment: Comment: Matching Gencode annotations to Assemblies
updated 8 months ago by 40k • written 8.3 years ago by ★ 4.2k
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0
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3.6k
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Comment: C: Illumina BeadChip Replicate Probes
8.5 years ago by Ying W ★ 4.2k
0
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0
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6.9k
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Comment: C: Distribution Of Gene Size
8.5 years ago by Ying W ★ 4.2k
1
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1
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3.2k
views
Comment: C: What is the correct way to use GNU parallel with Primer3?
8.5 years ago by Ying W ★ 4.2k
0
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0
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1.7k
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Comment: C: Unpacking reference file for Isaac Aligner
8.5 years ago by Ying W ★ 4.2k
0
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1
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4.3k
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Comment: Comment: problems in Diffbind In Creating Diffbind Object In R For Chip-Seq Peaks
updated 17 months ago by 40k • written 8.6 years ago by ★ 4.2k
179 results • Page 1 of 4
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