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Answer: A: Parsing raw Axiom .CEL files using affy2sv R package
8.4 years ago by Christian ★ 3.0k
2
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11k
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Answer: A: edgeR normalization method
8.4 years ago by Christian ★ 3.0k
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18k
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Comment: C: How Do Heterozygotes And Somatic Mutations Manifest In Sequencing Projects
8.4 years ago by Christian ★ 3.0k
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1
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18k
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Comment: C: GSEA Preranked analysis on RNA-SEQ
8.4 years ago by Christian ★ 3.0k
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3.1k
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Comment: C: SNP listed on dbSNP website but not in VCF
8.5 years ago by Christian ★ 3.0k
0
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32k
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Comment: C: How To Organize A Pipeline Of Small Scripts Together?
8.5 years ago by Christian ★ 3.0k
0
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1
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32k
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Comment: C: How To Organize A Pipeline Of Small Scripts Together?
8.5 years ago by Christian ★ 3.0k
0
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3.1k
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Comment: C: SNP listed on dbSNP website but not in VCF
8.6 years ago by Christian ★ 3.0k
1
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1
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1.4k
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Answer: A: How to see if DEGs are grouped in genome?
8.6 years ago by Christian ★ 3.0k
5
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2.4k
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Answer: A: needleman-wunsch (ggsearch implementation) not symmetric
8.6 years ago by Christian ★ 3.0k
3
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1
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25k
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Comment: C: Selection Of Background Gene Set In Enrichment Analysis
8.6 years ago by Christian ★ 3.0k
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1
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2.9k
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Answer: A: Next-generation DNA sequencing: How to tell systematic errors from real SNVs?
8.6 years ago by Christian ★ 3.0k
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2.0k
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Answer: A: How to can analyze the Affymetrix CytoscanHD array data?
8.7 years ago by Christian ★ 3.0k
0
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1
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25k
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Comment: C: Selection Of Background Gene Set In Enrichment Analysis
8.7 years ago by Christian ★ 3.0k
0
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2.9k
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Job: Bioinformatician/systems biologist at Children's Cancer Research Institute, Vienna
systems-biology
updated 16 months ago by 43k • written 8.8 years ago by ★ 3.0k
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1
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3.8k
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Comment: C: Hardware Recommendations: 1 Terabyte of RAM?
8.8 years ago by Christian ★ 3.0k
2
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1
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2.3k
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Answer: A: impact of recurrent SNVs?
8.8 years ago by Christian ★ 3.0k
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3.3k
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Comment: C: How to create a pooled normal exome sample?
8.8 years ago by Christian ★ 3.0k
0
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1
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3.8k
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Comment: C: Hardware Recommendations: 1 Terabyte of RAM?
8.8 years ago by Christian ★ 3.0k
0
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0
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1.9k
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Answer: A: categorising proteins into families when you have amino acid sequences
8.8 years ago by Christian ★ 3.0k
0
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0
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53k
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Comment: C: Should We Remove Duplicated Reads In Rna-Seq ?
8.8 years ago by Christian ★ 3.0k
1
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8.0k
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Comment: C: How to remove non-unique mapping reads with Hisat?
8.8 years ago by Christian ★ 3.0k
1
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0
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4.5k
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Comment: C: Inconsistent numbers when using Kegg pathway analysis via DAVID?
8.9 years ago by Christian ★ 3.0k
0
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0
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3.3k
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Comment: C: David enrichment analysis inconsistency
8.9 years ago by Christian ★ 3.0k
0
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1
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23k
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Comment: Comment: Are we tricking ourselves with batch effect correction?
updated 15 months ago by 43k • written 8.9 years ago by ★ 3.0k
0
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0
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23k
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Comment: Comment: Are we tricking ourselves with batch effect correction?
updated 15 months ago by 43k • written 8.9 years ago by ★ 3.0k
0
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0
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23k
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Comment: Comment: Are we tricking ourselves with batch effect correction?
updated 15 months ago by 43k • written 8.9 years ago by ★ 3.0k
0
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0
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5.7k
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Comment: C: How to read Affymetrix CYCHP File
8.9 years ago by Christian ★ 3.0k
0
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0
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5.9k
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Comment: C: Docker - one image to rule them all?
9.0 years ago by Christian ★ 3.0k
0
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0
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83k
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Comment: C: Drawing Chromosome Ideograms With Data
9.0 years ago by Christian ★ 3.0k
1
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0
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17k
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Comment: C: Workflow management software for pipeline development in NGS
9.0 years ago by Christian ★ 3.0k
80
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23
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5.3k
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11 follow
Forum: Are we facing a bioinformatician shortage?
salary career
updated 13 months ago by 43k • written 9.5 years ago by ★ 3.0k
0
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1
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2.1k
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Comment: C: QC on samples in a targeted NGS experiment
9.1 years ago by Christian ★ 3.0k
0
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0
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2.5k
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Answer: A: Genome Browse (Golden Helix) on a server/cluster X11 forwarded to Windows/Mac ma
9.2 years ago by Christian ★ 3.0k
2
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3
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7.5k
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Comment: C: How to compute physical per-base coverage from WGS paired-end reads?
9.2 years ago by Christian ★ 3.0k
13
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15
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7.5k
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8 follow
How to compute physical per-base coverage from WGS paired-end reads?
coverage WGS
updated 22 months ago by 43k • written 9.2 years ago by ★ 3.0k
0
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0
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7.5k
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Comment: Comment: How to compute physical per-base coverage from WGS paired-end reads?
updated 2.0 years ago by 43k • written 9.2 years ago by ★ 3.0k
0
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1
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7.5k
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Comment: Comment: How to compute physical per-base coverage from WGS paired-end reads?
updated 2.0 years ago by 43k • written 9.2 years ago by ★ 3.0k
0
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1
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7.5k
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Comment: C: How to compute empirical physical per-base coverage from WGS paired-end reads?
9.2 years ago by Christian ★ 3.0k
0
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0
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7.1k
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Comment: Comment: Counting The Whole Insert Size From Paired-End Reads As Coverage
updated 2.0 years ago by 43k • written 9.2 years ago by ★ 3.0k
0
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0
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2.0k
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Comment: C: lnkRNA gene names not recognized by DAVID
9.2 years ago by Christian ★ 3.0k
0
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0
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2.5k
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Comment: C: Genome Browse (Golden Helix) on a server/cluster X11 forwarded to Windows/Mac ma
9.2 years ago by Christian ★ 3.0k
1
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1
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2.5k
views
PathScan: How to control for gene-specific differences in background mutation rates?
pathway-analysis pathscan cancer genome-music
updated 2.1 years ago by 43k • written 9.4 years ago by ★ 3.0k
0
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0
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2.2k
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Comment: C: Cancer related Pathway Annotations
9.2 years ago by Christian ★ 3.0k
0
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0
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4.3k
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Answer: A: Any good offline zoomable genome browsers?
9.2 years ago by Christian ★ 3.0k
0
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0
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2.3k
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Comment: C: Differential copy number analysis
9.3 years ago by Christian ★ 3.0k
0
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1
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2.3k
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Answer: Answer: Differential copy number analysis
updated 2.1 years ago by 43k • written 9.3 years ago by ★ 3.0k
0
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0
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6.2k
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Comment: C: RNA-seq: Adjust library size using total uniquely mappable tags or only reads th
9.3 years ago by Christian ★ 3.0k
0
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0
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3.4k
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Comment: C: exome cnv analysis of cases only
9.3 years ago by Christian ★ 3.0k
1
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1
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3.0k
views
Comment: C: Studying Bioinformatics - Reasons, motives and career
9.4 years ago by Christian ★ 3.0k
224 results • Page 2 of 5
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