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Comment: Comment: Fast genotyping for PRS calculation
3.7 years ago by German.M.Demidov ★ 3.0k
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2
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956
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Fast genotyping for PRS calculation
PRS
3.7 years ago by German.M.Demidov ★ 3.0k
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787
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Comment: Comment: How Can I Identify DMRs in RRBS samples?
3.7 years ago by German.M.Demidov ★ 3.0k
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0
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808
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Comment: Comment: Is there a familial cancer database?
3.7 years ago by German.M.Demidov ★ 3.0k
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1
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4.6k
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Comment: Comment: Convert 4 million SNPs' positions to rsID
3.7 years ago by German.M.Demidov ★ 3.0k
2
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1
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1.3k
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Comment: Comment: CADD score
3.7 years ago by German.M.Demidov ★ 3.0k
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0
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942
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Comment: Comment: clustering samples
3.7 years ago by German.M.Demidov ★ 3.0k
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0
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948
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Comment: Comment: calculate genome intron length
3.7 years ago by German.M.Demidov ★ 3.0k
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0
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991
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Comment: Comment: How to detect CNV via readDepth with multiple samples
3.7 years ago by German.M.Demidov ★ 3.0k
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1
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5.1k
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Comment: Comment: Error in R command running in my server
3.7 years ago by German.M.Demidov ★ 3.0k
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1
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5.1k
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Comment: Comment: Error in R command running in my server
3.7 years ago by German.M.Demidov ★ 3.0k
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0
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1.2k
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Comment: Comment: What is duplicate reads in sequencing?
3.7 years ago by German.M.Demidov ★ 3.0k
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1
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2.4k
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Comment: Comment: How should I normalize a dataset for non-normally distributed, zero-inflated, an
3.7 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.4k
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Comment: Comment: How should I normalize a dataset for non-normally distributed, zero-inflated, an
3.7 years ago by German.M.Demidov ★ 3.0k
1
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1
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3.1k
views
Comment: Comment: Inflated p-values in QQ-plot
3.7 years ago by German.M.Demidov ★ 3.0k
1
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1
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3.1k
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Comment: Comment: Inflated p-values in QQ-plot
3.7 years ago by German.M.Demidov ★ 3.0k
1
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1
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3.1k
views
Comment: Comment: Inflated p-values in QQ-plot
3.7 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.7k
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Comment: Comment: How to know if my insert size distribution is normal?
3.7 years ago by German.M.Demidov ★ 3.0k
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0
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2.1k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.1k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.1k
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Comment: Comment: RNA-Seq, mutation , copy numnber
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.1k
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Comment: Comment: Extract allelic depths in a BAM
3.8 years ago by German.M.Demidov ★ 3.0k
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0
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1.6k
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Comment: Comment: Very high variant similarity between a couple
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.6k
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Comment: Comment: Very high variant similarity between a couple
3.8 years ago by German.M.Demidov ★ 3.0k
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0
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2.1k
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Comment: Comment: SNPs significant in all Plink tests
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.1k
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Comment: Comment: SNPs significant in all Plink tests
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.1k
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Comment: Comment: SNPs significant in all Plink tests
3.8 years ago by German.M.Demidov ★ 3.0k
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1
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2.1k
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Comment: Comment: SNPs significant in all Plink tests
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.4k
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Comment: Comment: Meaning of allele frequency
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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779
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Comment: Comment: low coverage genome compare to the exome with respect to the level of coverage a
3.8 years ago by German.M.Demidov ★ 3.0k
3
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1
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1.4k
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Comment: Comment: 60X coverage_genomic coverage vary
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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1.1k
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Comment: Comment: How to edit a VCF file in python
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
reply
1.7k
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Comment: Comment: CNV detection for amplicon sequence datas without bed file
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.2k
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Comment: Comment: CNV calling, copy number calling, using ONLY Log2R values (with segmentation
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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910
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Comment: Comment: Fisher test in R to compare percentages of three databases
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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848
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Comment: Comment: Reference material for distinguishing focal CNV and chromosome CNV
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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6.0k
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Comment: Comment: Copy Number Variation Tools
3.8 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.0k
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Comment: Comment: How to get copy number of gene from WGS data?
3.9 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.4k
views
Comment: Comment: HPO Terms using OMIM IDs
3.9 years ago by German.M.Demidov ★ 3.0k
0
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0
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886
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Array variant to reference-standard way
genotyping
4.0 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.0k
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Comment: Comment: Isolate a Region in a Vcf File to make a Smaller Vcf File
4.1 years ago by German.M.Demidov ★ 3.0k
0
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0
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7.1k
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Comment: Comment: Problem with viewing BAM files in IGV
4.1 years ago by German.M.Demidov ★ 3.0k
1
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1
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7.1k
views
Comment: Comment: Problem with viewing BAM files in IGV
4.1 years ago by German.M.Demidov ★ 3.0k
0
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1
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7.1k
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Comment: Comment: Problem with viewing BAM files in IGV
4.1 years ago by German.M.Demidov ★ 3.0k
1
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0
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2.1k
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Comment: Comment: Why some SNP's are not assigned to any gene?
4.1 years ago by German.M.Demidov ★ 3.0k
0
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0
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4.6k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
4.1 years ago by German.M.Demidov ★ 3.0k
2
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1
reply
2.1k
views
Comment: Comment: Why some SNP's are not assigned to any gene?
4.1 years ago by German.M.Demidov ★ 3.0k
0
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0
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1.8k
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Comment: Comment: Dragen-gatk pipeline information ?
4.1 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.8k
views
Comment: Comment: Dragen-gatk pipeline information ?
4.1 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.3k
views
Comment: Comment: custom reference panel
4.1 years ago by German.M.Demidov ★ 3.0k
657 results • Page 2 of 14
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