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Comment: Comment: Why GC content is important on NIPT results?
3.6 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.4k
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Comment: Comment: Why GC content is important on NIPT results?
3.6 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.7k
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Comment: Comment: What Coverage allele-fraction threshold to use?
3.6 years ago by German.M.Demidov ★ 2.9k
0
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0
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2.1k
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Comment: Comment: ExomeDepth negative BF (bayesian factor) values meaning
3.6 years ago by German.M.Demidov ★ 2.9k
4
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2
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7.3k
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Comment: Comment: What is gnomAD allele frequency
3.6 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.7k
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Comment: Comment: What Coverage allele-fraction threshold to use?
3.6 years ago by German.M.Demidov ★ 2.9k
1
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1
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1.4k
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Comment: Comment: Where to get consensus sequences of human transposable elements
3.6 years ago by German.M.Demidov ★ 2.9k
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0
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1.0k
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Comment: Comment: Help with statistic model
3.6 years ago by German.M.Demidov ★ 2.9k
0
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0
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3.5k
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Comment: Comment: Any standalone tool for INDEL Realignment?
3.6 years ago by German.M.Demidov ★ 2.9k
0
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0
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846
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Comment: Comment: MSI cslculation
3.7 years ago by German.M.Demidov ★ 2.9k
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1
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2.3k
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Comment: Comment: Important genes are not differentially expressed
3.7 years ago by German.M.Demidov ★ 2.9k
1
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1
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2.3k
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Answer: Answer: Important genes are not differentially expressed
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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989
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Comment: Comment: Asking for papers: rare variants of potentially moderate impact
3.7 years ago by German.M.Demidov ★ 2.9k
1
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2
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989
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Asking for papers: rare variants of potentially moderate impact
human disease genetics
3.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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820
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Comment: Comment: Use of megSAP
3.7 years ago by German.M.Demidov ★ 2.9k
1
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0
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698
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Comment: Comment: Reasons for drops in alignment
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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755
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Comment: Comment: Mendelian vs Inherited variants
3.7 years ago by German.M.Demidov ★ 2.9k
3
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1
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1.7k
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Answer: Comment: GWAS Summary statistic
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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822
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Comment: Comment: Risk calculation in pedigrees
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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2.5k
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Comment: Comment: IDT xGen Exome Research Panel v2 vs Twist Human exome core
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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822
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Comment: Comment: Risk calculation in pedigrees
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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1.1k
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Comment: C: Power of differential expression for a single gene analysis
3.7 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: C: Power of differential expression for a single gene analysis
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.1k
views
Comment: C: Power of differential expression for a single gene analysis
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.1k
views
Comment: C: Power of differential expression for a single gene analysis
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
reply
1.1k
views
Comment: C: Power of differential expression for a single gene analysis
3.7 years ago by German.M.Demidov ★ 2.9k
6
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10
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1.1k
views
Power of differential expression for a single gene analysis
RNA-Seq
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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2.5k
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Comment: C: plink : Batch effect issues after merge of two datasets
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.5k
views
Comment: C: plink : Batch effect issues after merge of two datasets
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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1.5k
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Comment: C: How to calculate p-values from PLINK output by hand
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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2.5k
views
Comment: C: plink : Batch effect issues after merge of two datasets
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
reply
1.5k
views
Comment: C: How to calculate p-values from PLINK output by hand
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.5k
views
Comment: C: How to calculate p-values from PLINK output by hand
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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749
views
Comment: C: [WGS] how to correctly visualize long indels (50nt+)
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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702
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Comment: C: Violation of Independence test for differential methylation (DM)
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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636
views
Comment: C: How can I detect small deletion
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
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994
views
Comment: C: How to draw survival curve marked at one censoring time for each patient
3.7 years ago by German.M.Demidov ★ 2.9k
0
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1
reply
994
views
Comment: C: How to draw survival curve marked at one censoring time for each patient
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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7.4k
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Comment: C: Split multiallelic SNPs to biallelic from vcf
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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762
views
Comment: C: How to convert WGS data to microarray format?
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
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497
views
Horizontal sub-windows for IGV
IGV bam
3.7 years ago by German.M.Demidov ★ 2.9k
0
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0
replies
598
views
Genotyping: array variants from WGS
array WGS
3.9 years ago by German.M.Demidov ★ 2.9k
0
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0
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825
views
Deviance in allele frequencies between arrays and WGS
GWAS PRS WGS array
3.9 years ago by German.M.Demidov ★ 2.9k
24
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26
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4.1k
views
Tool: ClinCNV: CNV detection from short reads
variant-calling cna cnv
updated 17 months ago by 44k • written 5.1 years ago by ★ 2.9k
1
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0
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1.2k
views
Comment: C: Is it possible to infer tumor purity from tumor-specific Variant Allele Fraction
4.0 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.6k
views
Comment: C: Phylogenetic tree for CNVs
4.0 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.6k
views
Comment: C: Phylogenetic tree for CNVs
4.0 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.6k
views
Comment: C: Phylogenetic tree for CNVs
4.0 years ago by German.M.Demidov ★ 2.9k
0
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1
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1.6k
views
Comment: C: Phylogenetic tree for CNVs
4.0 years ago by German.M.Demidov ★ 2.9k
0
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0
replies
3.1k
views
Comment: C: Help with CNV calling using ExomeDepth
4.0 years ago by German.M.Demidov ★ 2.9k
656 results • Page 5 of 14
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