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540
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Fast genotyping for PRS calculation
PRS
2.2 years ago by German.M.Demidov ★ 2.9k
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0
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456
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Comment: Comment: How Can I Identify DMRs in RRBS samples?
2.2 years ago by German.M.Demidov ★ 2.9k
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0
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522
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Comment: Comment: Is there a familial cancer database?
2.2 years ago by German.M.Demidov ★ 2.9k
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1
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3.1k
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Comment: Comment: Convert 4 million SNPs' positions to rsID
2.2 years ago by German.M.Demidov ★ 2.9k
2
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1
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773
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Comment: Comment: CADD score
2.2 years ago by German.M.Demidov ★ 2.9k
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587
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Comment: Comment: clustering samples
2.2 years ago by German.M.Demidov ★ 2.9k
1
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0
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570
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Comment: Comment: calculate genome intron length
2.2 years ago by German.M.Demidov ★ 2.9k
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0
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579
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Comment: Comment: How to detect CNV via readDepth with multiple samples
2.2 years ago by German.M.Demidov ★ 2.9k
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1
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3.5k
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Comment: Comment: Error in R command running in my server
2.2 years ago by German.M.Demidov ★ 2.9k
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1
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3.5k
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Comment: Comment: Error in R command running in my server
2.2 years ago by German.M.Demidov ★ 2.9k
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0
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697
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Comment: Comment: What is duplicate reads in sequencing?
2.2 years ago by German.M.Demidov ★ 2.9k
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1
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1.5k
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Comment: Comment: How should I normalize a dataset for non-normally distributed, zero-inflated, an
2.2 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.5k
views
Comment: Comment: How should I normalize a dataset for non-normally distributed, zero-inflated, an
2.2 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.6k
views
Comment: Comment: Inflated p-values in QQ-plot
2.2 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.6k
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Comment: Comment: Inflated p-values in QQ-plot
2.2 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.6k
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Comment: Comment: Inflated p-values in QQ-plot
2.2 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.1k
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Comment: Comment: How to know if my insert size distribution is normal?
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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1.3k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.3k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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721
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Comment: Comment: RNA-Seq, mutation , copy numnber
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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691
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Comment: Comment: Extract allelic depths in a BAM
2.3 years ago by German.M.Demidov ★ 2.9k
1
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0
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959
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Comment: Comment: Very high variant similarity between a couple
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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959
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Comment: Comment: Very high variant similarity between a couple
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
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1
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1.2k
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Comment: Comment: SNPs significant in all Plink tests
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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898
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Comment: Comment: Meaning of allele frequency
2.3 years ago by German.M.Demidov ★ 2.9k
0
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0
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466
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Comment: Comment: low coverage genome compare to the exome with respect to the level of coverage a
2.3 years ago by German.M.Demidov ★ 2.9k
3
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1
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818
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Comment: Comment: 60X coverage_genomic coverage vary
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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685
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Comment: Comment: How to edit a VCF file in python
2.3 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.1k
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Comment: Comment: CNV detection for amplicon sequence datas without bed file
2.3 years ago by German.M.Demidov ★ 2.9k
1
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0
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691
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Comment: Comment: CNV calling, copy number calling, using ONLY Log2R values (with segmentation
2.3 years ago by German.M.Demidov ★ 2.9k
1
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0
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542
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Comment: Comment: Fisher test in R to compare percentages of three databases
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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503
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Comment: Comment: Reference material for distinguishing focal CNV and chromosome CNV
2.3 years ago by German.M.Demidov ★ 2.9k
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0
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4.7k
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Comment: Comment: Copy Number Variation Tools
2.3 years ago by German.M.Demidov ★ 2.9k
1
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0
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652
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Comment: Comment: How to get copy number of gene from WGS data?
2.4 years ago by German.M.Demidov ★ 2.9k
1
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1
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885
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Comment: Comment: HPO Terms using OMIM IDs
2.4 years ago by German.M.Demidov ★ 2.9k
0
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0
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499
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Array variant to reference-standard way
genotyping
2.6 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.3k
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Comment: Comment: Isolate a Region in a Vcf File to make a Smaller Vcf File
2.6 years ago by German.M.Demidov ★ 2.9k
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0
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3.3k
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Comment: Comment: Problem with viewing BAM files in IGV
2.6 years ago by German.M.Demidov ★ 2.9k
1
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1
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3.3k
views
Comment: Comment: Problem with viewing BAM files in IGV
2.6 years ago by German.M.Demidov ★ 2.9k
0
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1
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3.3k
views
Comment: Comment: Problem with viewing BAM files in IGV
2.6 years ago by German.M.Demidov ★ 2.9k
1
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0
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1.4k
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Comment: Comment: Why some SNP's are not assigned to any gene?
2.6 years ago by German.M.Demidov ★ 2.9k
0
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0
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3.1k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
2.6 years ago by German.M.Demidov ★ 2.9k
2
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1
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1.4k
views
Comment: Comment: Why some SNP's are not assigned to any gene?
2.6 years ago by German.M.Demidov ★ 2.9k
0
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0
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1.2k
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Comment: Comment: Dragen-gatk pipeline information ?
2.6 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.2k
views
Comment: Comment: Dragen-gatk pipeline information ?
2.6 years ago by German.M.Demidov ★ 2.9k
1
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1
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722
views
Comment: Comment: custom reference panel
2.6 years ago by German.M.Demidov ★ 2.9k
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0
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2.4k
views
Comment: Comment: Filtering long indels from VCF
2.6 years ago by German.M.Demidov ★ 2.9k
661 results • Page 2 of 14
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