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Comment:
Comment: A question about the missing or not observed alleles in PLINK datasets
5 months ago by
abedkurdi10
▴ 190
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921
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Comment:
Comment: A question about genotyping rate
6 months ago by
abedkurdi10
▴ 190
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921
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Comment:
Comment: A question about genotyping rate
6 months ago by
abedkurdi10
▴ 190
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921
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Comment:
Comment: A question about genotyping rate
6 months ago by
abedkurdi10
▴ 190
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756
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Comment:
Comment: DESeq2 analysis using two featureCounts generated from different studies
7 months ago by
abedkurdi10
▴ 190
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5.8k
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Comment:
Comment: Trouble setting "ident" argument in FindMarkers in Seurat
19 months ago by
abedkurdi10
▴ 190
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1
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1.2k
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Comment:
Comment: SNP downstream analysis
2.1 years ago by
abedkurdi10
▴ 190
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1.1k
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Comment:
Comment: SRA dataset to Seurat Object
2.1 years ago by
abedkurdi10
▴ 190
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1
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886
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Comment:
Comment: HT-Seq, Gene ID appeared in Gene Name row
2.2 years ago by
abedkurdi10
▴ 190
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1
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1.1k
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Comment:
Comment: SRA dataset to Seurat Object
2.2 years ago by
abedkurdi10
▴ 190
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2.0k
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Comment:
Comment: How to label gene ID on volcano plot?
2.2 years ago by
abedkurdi10
▴ 190
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2.0k
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Comment:
Comment: How to label gene ID on volcano plot?
2.2 years ago by
abedkurdi10
▴ 190
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2.0k
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Comment:
Comment: How to label gene ID on volcano plot?
2.2 years ago by
abedkurdi10
▴ 190
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1
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962
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Comment:
Comment: VariantsToTable not produce output file
2.2 years ago by
abedkurdi10
▴ 190
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1
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1.1k
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Comment:
Comment: filter and annotate vcf file
2.2 years ago by
abedkurdi10
▴ 190
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1.2k
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Comment:
Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
2.2 years ago by
abedkurdi10
▴ 190
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1.9k
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Comment:
Comment: How can I download the VCF file of the 1000 genomes project with the population
2.2 years ago by
abedkurdi10
▴ 190
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1.2k
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Comment:
Comment: Existing tutorials using Docker to set up and run any type of NGS workflow?
2.2 years ago by
abedkurdi10
▴ 190
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624
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Comment:
Comment: Variant Annotation Integrator VCF File
2.2 years ago by
abedkurdi10
▴ 190
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625
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Comment:
Comment: convert unmapped bam to fastqs and preserve tag
2.2 years ago by
abedkurdi10
▴ 190
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955
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Comment:
Comment: gene ID RNAseq
2.2 years ago by
abedkurdi10
▴ 190
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647
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Comment:
Comment: Find a position in IGV when variant is giving in the format gene_name 12345-1G>
2.2 years ago by
abedkurdi10
▴ 190
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1
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955
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Comment:
Comment: gene ID RNAseq
2.2 years ago by
abedkurdi10
▴ 190
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0
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513
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Comment:
Comment: VEP and future analysis
2.2 years ago by
abedkurdi10
▴ 190
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1
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955
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Comment:
Comment: gene ID RNAseq
2.2 years ago by
abedkurdi10
▴ 190
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1.6k
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Comment:
Comment: seurat dotplot issue
2.2 years ago by
abedkurdi10
▴ 190
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770
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Comment:
Comment: Data sets of WGS + disease phenotypes?
2.3 years ago by
abedkurdi10
▴ 190
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0
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959
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Comment:
Comment: getting indexing files using hisat2-build
2.3 years ago by
abedkurdi10
▴ 190
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0
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657
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Comment:
Comment: Rsubread: Aligning multiple single and paired-end reads from multiple files (lan
2.3 years ago by
abedkurdi10
▴ 190
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0
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5.8k
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Comment:
Comment: Trouble setting "ident" argument in FindMarkers in Seurat
2.3 years ago by
abedkurdi10
▴ 190
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0
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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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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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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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0
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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
0
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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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0
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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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0
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1.2k
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Comment:
C: Bigwig circular plot
4.0 years ago by
abedkurdi10
▴ 190
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0
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2.1k
views
Comment:
C: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by
abedkurdi10
▴ 190
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1
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2.1k
views
Comment:
C: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by
abedkurdi10
▴ 190
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votes
1
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2.1k
views
Comment:
A: Replace the bases with N for the sites with evidence of a SNP
4.9 years ago by
abedkurdi10
▴ 190
0
votes
2
replies
2.3k
views
Comment:
C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by
abedkurdi10
▴ 190
0
votes
1
reply
2.3k
views
Comment:
C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by
abedkurdi10
▴ 190
0
votes
0
replies
2.3k
views
Comment:
C: Optimal number of samples needed to detect a variant from panel sequencing
7.2 years ago by
abedkurdi10
▴ 190
0
votes
0
replies
2.2k
views
Comment:
C: Statistics on BED files
7.3 years ago by
abedkurdi10
▴ 190
0
votes
1
reply
3.9k
views
Comment:
C: Thresholds to filter out variants from vcf file
7.5 years ago by
abedkurdi10
▴ 190
0
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1
reply
3.9k
views
Comment:
C: Thresholds to filter out variants from vcf file
7.5 years ago by
abedkurdi10
▴ 190
1
vote
0
replies
4.6k
views
Comment:
C: VCF file re-header
7.5 years ago by
abedkurdi10
▴ 190
0
votes
1
reply
4.6k
views
Comment:
C: VCF file re-header
7.5 years ago by
abedkurdi10
▴ 190
0
votes
0
replies
4.4k
views
Comment:
C: Clinical significance explanation
7.5 years ago by
abedkurdi10
▴ 190
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