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Answer: Answer: Heatmap in ggplot
3.6 years ago by abedkurdi10 ▴ 190
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Answer: Answer: eagle2 + minimac4 script for phasing and imputation
3.6 years ago by abedkurdi10 ▴ 190
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Comment: Comment: Data sets of WGS + disease phenotypes?
3.7 years ago by abedkurdi10 ▴ 190
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948
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Answer: Answer: Single cell Sequencing
3.7 years ago by abedkurdi10 ▴ 190
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1.3k
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Comment: Comment: getting indexing files using hisat2-build
3.7 years ago by abedkurdi10 ▴ 190
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1.9k
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Answer: Answer: SNP downstream analysis
3.7 years ago by abedkurdi10 ▴ 190
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Comment: Comment: Rsubread: Aligning multiple single and paired-end reads from multiple files (lan
3.7 years ago by abedkurdi10 ▴ 190
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1.3k
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Answer: Answer: Data sets of WGS + disease phenotypes?
3.7 years ago by abedkurdi10 ▴ 190
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11k
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Comment: Comment: Trouble setting "ident" argument in FindMarkers in Seurat
3.7 years ago by abedkurdi10 ▴ 190
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1
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1.7k
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Answer: Answer: Where I can get pipeline for covid genome assembly?
3.7 years ago by abedkurdi10 ▴ 190
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1.9k
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Answer: Answer: Downstream analysis of VCF file
3.7 years ago by abedkurdi10 ▴ 190
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6.2k
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Answer: Answer: Seurat orig.ident
3.7 years ago by abedkurdi10 ▴ 190
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6.9k
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Comment: Comment: Finding Subclusters in Seurat Clusters
3.9 years ago by abedkurdi10 ▴ 190
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39k
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Comment: Comment: Batch correction in DESeq2
3.9 years ago by abedkurdi10 ▴ 190
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1
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6.9k
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Comment: Comment: Finding Subclusters in Seurat Clusters
4.0 years ago by abedkurdi10 ▴ 190
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1
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2.1k
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Answer: A: How to call CNV without normal samples
4.8 years ago by abedkurdi10 ▴ 190
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2.1k
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Answer: A: intersect two file
4.8 years ago by abedkurdi10 ▴ 190
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4
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1.5k
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RNA-seq Infer experiment wrong strandeness information
RNA-Seq rseqc infer_experiment
5.2 years ago by abedkurdi10 ▴ 190
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1.5k
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Answer: A: RNA-seq Infer experiment wrong strandeness information
5.2 years ago by abedkurdi10 ▴ 190
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1.5k
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Comment: C: RNA-seq Infer experiment wrong strandeness information
5.2 years ago by abedkurdi10 ▴ 190
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3.5k
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Comment: C: Interval list for GATK tool Haplotype Caller
5.3 years ago by abedkurdi10 ▴ 190
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3.5k
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Answer: A: Interval list for GATK tool Haplotype Caller
5.3 years ago by abedkurdi10 ▴ 190
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1
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5.1k
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Comment: C: Conversion of Vep.vcf to MAF format?
5.3 years ago by abedkurdi10 ▴ 190
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5.1k
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Comment: C: Conversion of Vep.vcf to MAF format?
5.3 years ago by abedkurdi10 ▴ 190
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5.1k
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Answer: A: Conversion of Vep.vcf to MAF format?
5.3 years ago by abedkurdi10 ▴ 190
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1.7k
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Comment: C: Bigwig circular plot
5.4 years ago by abedkurdi10 ▴ 190
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2
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1.7k
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Bigwig circular plot
bigwig javascript java
updated 2.3 years ago by 45k • written 5.4 years ago by ▴ 190
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3.0k
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Comment: C: Replace the bases with N for the sites with evidence of a SNP
6.3 years ago by abedkurdi10 ▴ 190
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3.0k
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Comment: C: Replace the bases with N for the sites with evidence of a SNP
6.3 years ago by abedkurdi10 ▴ 190
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1
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3.0k
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Comment: A: Replace the bases with N for the sites with evidence of a SNP
6.3 years ago by abedkurdi10 ▴ 190
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2
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3.1k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
8.6 years ago by abedkurdi10 ▴ 190
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1
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3.1k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
8.6 years ago by abedkurdi10 ▴ 190
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3.1k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
8.6 years ago by abedkurdi10 ▴ 190
4
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10
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3.1k
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Optimal number of samples needed to detect a variant from panel sequencing
exome sequencing variants samples
8.6 years ago by abedkurdi10 ▴ 190
3
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1
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1.8k
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Error in Rscript
R error Rscript
updated 8.6 years ago by 36k • written 8.6 years ago by ▴ 190
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2.5k
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Comment: C: Statistics on BED files
8.7 years ago by abedkurdi10 ▴ 190
2
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2
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2.5k
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Statistics on BED files
bed statistics intervals
updated 8.7 years ago by 36k • written 8.7 years ago by ▴ 190
5
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6
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4.7k
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Thresholds to filter out variants from vcf file
vcf thresholds filtering
updated 8.9 years ago by ★ 1.2k • written 8.9 years ago by ▴ 190
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4.7k
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Comment: C: Thresholds to filter out variants from vcf file
8.9 years ago by abedkurdi10 ▴ 190
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4.7k
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Comment: C: Thresholds to filter out variants from vcf file
8.9 years ago by abedkurdi10 ▴ 190
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5.0k
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Comment: C: VCF file re-header
8.9 years ago by abedkurdi10 ▴ 190
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5.0k
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Comment: C: VCF file re-header
8.9 years ago by abedkurdi10 ▴ 190
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5.0k
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VCF file re-header
vcf header vcf reheader
8.9 years ago by abedkurdi10 ▴ 190
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5.4k
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Comment: C: Clinical significance explanation
8.9 years ago by abedkurdi10 ▴ 190
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5.4k
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Comment: C: Clinical significance explanation
8.9 years ago by abedkurdi10 ▴ 190
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6
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5.4k
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Clinical significance explanation
clinvar clinical significance
updated 8.9 years ago by 105k • written 8.9 years ago by ▴ 190
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4.1k
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Comment: C: Realigner Target Creator
9.0 years ago by abedkurdi10 ▴ 190
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1
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4.1k
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Answer: A: Realigner Target Creator
9.0 years ago by abedkurdi10 ▴ 190
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37k
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Comment: C: How bcftools isec works ?
9.0 years ago by abedkurdi10 ▴ 190
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5.0k
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raw data (fastq files) of whole exome sequencing (WES) of somatic mutations
somatic wes samples
updated 9.1 years ago by 9.8k • written 9.1 years ago by ▴ 190
100 results • Page 2 of 2
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