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29k
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Comment: Comment: Batch correction in DESeq2
2.6 years ago by abedkurdi10 ▴ 190
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1
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5.6k
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Comment: Comment: Finding Subclusters in Seurat Clusters
2.6 years ago by abedkurdi10 ▴ 190
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1.3k
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Answer: A: How to call CNV without normal samples
3.5 years ago by abedkurdi10 ▴ 190
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1.3k
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Answer: A: intersect two file
3.5 years ago by abedkurdi10 ▴ 190
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4
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955
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RNA-seq Infer experiment wrong strandeness information
RNA-Seq rseqc infer_experiment
3.8 years ago by abedkurdi10 ▴ 190
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1
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955
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Answer: A: RNA-seq Infer experiment wrong strandeness information
3.8 years ago by abedkurdi10 ▴ 190
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0
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955
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Comment: C: RNA-seq Infer experiment wrong strandeness information
3.8 years ago by abedkurdi10 ▴ 190
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2.6k
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Comment: C: Interval list for GATK tool Haplotype Caller
3.9 years ago by abedkurdi10 ▴ 190
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1
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2.6k
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Answer: A: Interval list for GATK tool Haplotype Caller
3.9 years ago by abedkurdi10 ▴ 190
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1
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3.6k
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Comment: C: Conversion of Vep.vcf to MAF format?
3.9 years ago by abedkurdi10 ▴ 190
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3.6k
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Comment: C: Conversion of Vep.vcf to MAF format?
3.9 years ago by abedkurdi10 ▴ 190
1
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1
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3.6k
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Answer: A: Conversion of Vep.vcf to MAF format?
3.9 years ago by abedkurdi10 ▴ 190
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1.2k
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Comment: C: Bigwig circular plot
4.0 years ago by abedkurdi10 ▴ 190
0
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2
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1.2k
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Bigwig circular plot
bigwig javascript java
updated 10 months ago by 43k • written 4.1 years ago by ▴ 190
0
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0
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2.1k
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Comment: C: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by abedkurdi10 ▴ 190
0
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1
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2.1k
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Comment: C: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by abedkurdi10 ▴ 190
0
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1
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2.1k
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Comment: A: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by abedkurdi10 ▴ 190
0
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2
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2.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by abedkurdi10 ▴ 190
0
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1
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2.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by abedkurdi10 ▴ 190
0
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0
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2.3k
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Comment: C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by abedkurdi10 ▴ 190
4
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10
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2.3k
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Optimal number of samples needed to detect a variant from panel sequencing
exome sequencing variants samples
7.2 years ago by abedkurdi10 ▴ 190
3
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1
reply
1.5k
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Error in Rscript
R error Rscript
updated 7.2 years ago by 35k • written 7.2 years ago by ▴ 190
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0
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2.2k
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Comment: C: Statistics on BED files
7.3 years ago by abedkurdi10 ▴ 190
2
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2
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2.2k
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Statistics on BED files
bed statistics intervals
updated 7.3 years ago by 35k • written 7.3 years ago by ▴ 190
5
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6
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3.9k
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Thresholds to filter out variants from vcf file
vcf thresholds filtering
updated 7.5 years ago by ★ 1.2k • written 7.5 years ago by ▴ 190
0
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1
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3.9k
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Comment: C: Thresholds to filter out variants from vcf file
7.5 years ago by abedkurdi10 ▴ 190
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1
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3.9k
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Comment: C: Thresholds to filter out variants from vcf file
7.5 years ago by abedkurdi10 ▴ 190
1
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0
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4.6k
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Comment: C: VCF file re-header
7.5 years ago by abedkurdi10 ▴ 190
0
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1
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4.6k
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Comment: C: VCF file re-header
7.5 years ago by abedkurdi10 ▴ 190
2
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4
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4.6k
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VCF file re-header
vcf header vcf reheader
7.5 years ago by abedkurdi10 ▴ 190
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0
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4.4k
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Comment: C: Clinical significance explanation
7.5 years ago by abedkurdi10 ▴ 190
0
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1
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4.4k
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Comment: C: Clinical significance explanation
7.5 years ago by abedkurdi10 ▴ 190
0
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6
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4.4k
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Clinical significance explanation
clinvar clinical significance
updated 7.5 years ago by 104k • written 7.5 years ago by ▴ 190
0
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0
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3.5k
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Comment: C: Realigner Target Creator
7.6 years ago by abedkurdi10 ▴ 190
1
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1
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3.5k
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Answer: A: Realigner Target Creator
7.6 years ago by abedkurdi10 ▴ 190
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1
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28k
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Comment: C: How bcftools isec works ?
7.7 years ago by abedkurdi10 ▴ 190
0
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1
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4.6k
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raw data (fastq files) of whole exome sequencing (WES) of somatic mutations
somatic wes samples
updated 7.7 years ago by 9.7k • written 7.7 years ago by ▴ 190
87 results • Page 2 of 2
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