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2
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Fast genotyping for PRS calculation
PRS
3.3 years ago by German.M.Demidov ★ 3.0k
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0
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680
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Comment: Comment: How Can I Identify DMRs in RRBS samples?
3.3 years ago by German.M.Demidov ★ 3.0k
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0
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713
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Comment: Comment: Is there a familial cancer database?
3.3 years ago by German.M.Demidov ★ 3.0k
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1
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4.2k
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Comment: Comment: Convert 4 million SNPs' positions to rsID
3.3 years ago by German.M.Demidov ★ 3.0k
2
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1
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1.1k
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Comment: Comment: CADD score
3.3 years ago by German.M.Demidov ★ 3.0k
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0
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838
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Comment: Comment: clustering samples
3.3 years ago by German.M.Demidov ★ 3.0k
1
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0
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828
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Comment: Comment: calculate genome intron length
3.3 years ago by German.M.Demidov ★ 3.0k
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0
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881
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Comment: Comment: How to detect CNV via readDepth with multiple samples
3.3 years ago by German.M.Demidov ★ 3.0k
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1
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4.7k
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Comment: Comment: Error in R command running in my server
3.3 years ago by German.M.Demidov ★ 3.0k
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1
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4.7k
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Comment: Comment: Error in R command running in my server
3.3 years ago by German.M.Demidov ★ 3.0k
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0
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1.0k
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Comment: Comment: What is duplicate reads in sequencing?
3.3 years ago by German.M.Demidov ★ 3.0k
0
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1
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2.2k
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Comment: Comment: How should I normalize a dataset for non-normally distributed, zero-inflated, an
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.2k
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Comment: Comment: How should I normalize a dataset for non-normally distributed, zero-inflated, an
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.7k
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Comment: Comment: Inflated p-values in QQ-plot
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.7k
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Comment: Comment: Inflated p-values in QQ-plot
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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2.7k
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Comment: Comment: Inflated p-values in QQ-plot
3.4 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.5k
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Comment: Comment: How to know if my insert size distribution is normal?
3.4 years ago by German.M.Demidov ★ 3.0k
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0
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1.8k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
3.4 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.8k
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Comment: Comment: How to interpret arcs in the Sashimi plots (IGV)?
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.0k
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Comment: Comment: RNA-Seq, mutation , copy numnber
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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980
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Comment: Comment: Extract allelic depths in a BAM
3.4 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.4k
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Comment: Comment: Very high variant similarity between a couple
3.4 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: Very high variant similarity between a couple
3.4 years ago by German.M.Demidov ★ 3.0k
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0
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1.8k
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Comment: Comment: SNPs significant in all Plink tests
3.4 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.8k
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Comment: Comment: SNPs significant in all Plink tests
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.8k
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Comment: Comment: SNPs significant in all Plink tests
3.4 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.8k
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Comment: Comment: SNPs significant in all Plink tests
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.2k
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Comment: Comment: Meaning of allele frequency
3.4 years ago by German.M.Demidov ★ 3.0k
0
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0
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679
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Comment: Comment: low coverage genome compare to the exome with respect to the level of coverage a
3.4 years ago by German.M.Demidov ★ 3.0k
3
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1
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1.2k
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Comment: Comment: 60X coverage_genomic coverage vary
3.4 years ago by German.M.Demidov ★ 3.0k
0
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0
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939
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Comment: Comment: How to edit a VCF file in python
3.4 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.5k
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Comment: Comment: CNV detection for amplicon sequence datas without bed file
3.4 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: CNV calling, copy number calling, using ONLY Log2R values (with segmentation
3.4 years ago by German.M.Demidov ★ 3.0k
1
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0
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789
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Comment: Comment: Fisher test in R to compare percentages of three databases
3.4 years ago by German.M.Demidov ★ 3.0k
0
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0
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730
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Comment: Comment: Reference material for distinguishing focal CNV and chromosome CNV
3.5 years ago by German.M.Demidov ★ 3.0k
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0
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5.6k
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Comment: Comment: Copy Number Variation Tools
3.5 years ago by German.M.Demidov ★ 3.0k
1
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0
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881
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Comment: Comment: How to get copy number of gene from WGS data?
3.5 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.2k
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Comment: Comment: HPO Terms using OMIM IDs
3.6 years ago by German.M.Demidov ★ 3.0k
0
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0
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797
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Array variant to reference-standard way
genotyping
3.7 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.9k
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Comment: Comment: Isolate a Region in a Vcf File to make a Smaller Vcf File
3.7 years ago by German.M.Demidov ★ 3.0k
0
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0
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6.2k
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Comment: Comment: Problem with viewing BAM files in IGV
3.7 years ago by German.M.Demidov ★ 3.0k
1
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1
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6.2k
views
Comment: Comment: Problem with viewing BAM files in IGV
3.7 years ago by German.M.Demidov ★ 3.0k
0
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1
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6.2k
views
Comment: Comment: Problem with viewing BAM files in IGV
3.7 years ago by German.M.Demidov ★ 3.0k
1
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0
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1.9k
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Comment: Comment: Why some SNP's are not assigned to any gene?
3.7 years ago by German.M.Demidov ★ 3.0k
0
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0
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4.3k
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Comment: Comment: Dealing with P value inflation of SNPs identified by qqplot
3.7 years ago by German.M.Demidov ★ 3.0k
2
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1
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1.9k
views
Comment: Comment: Why some SNP's are not assigned to any gene?
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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1.6k
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Comment: Comment: Dragen-gatk pipeline information ?
3.8 years ago by German.M.Demidov ★ 3.0k
0
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1
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1.6k
views
Comment: Comment: Dragen-gatk pipeline information ?
3.8 years ago by German.M.Demidov ★ 3.0k
1
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1
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1.0k
views
Comment: Comment: custom reference panel
3.8 years ago by German.M.Demidov ★ 3.0k
0
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0
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4.1k
views
Comment: Comment: Filtering long indels from VCF
3.8 years ago by German.M.Demidov ★ 3.0k
656 results • Page 2 of 14
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