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Comment: Comment: Prediction tools summary - zero values
13 months ago by luffy ▴ 130
1
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0
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794
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Comment: Comment: How to choose the best tool for variant trio analysis
13 months ago by luffy ▴ 130
3
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1
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1.4k
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Answer: Answer: Prediction tools summary - zero values
13 months ago by luffy ▴ 130
0
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1
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443
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small RNAseq analysis of non human samples
lncRNA sRNA DEG small-RNA RNA-seq
updated 13 months ago by 44k • written 13 months ago by ▴ 130
1
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0
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1.1k
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Comment: Comment: identify DEGs across all conditions and per specific conditions
14 months ago by luffy ▴ 130
1
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1
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1.0k
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Comment: Comment: Which function is best for pathway analysis?
14 months ago by luffy ▴ 130
1
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0
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676
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Answer: Answer: How to retrieve LoF and missense variants in WES data?
14 months ago by luffy ▴ 130
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0
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740
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Answer: Answer: functional and genome annotation analysis
14 months ago by luffy ▴ 130
0
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0
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1.2k
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Answer: Answer: matching gnomAD allele frequency
15 months ago by luffy ▴ 130
0
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0
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605
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Comment: Comment: Denovo variants
15 months ago by luffy ▴ 130
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1
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1.9k
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Comment: Comment: How to modify labels of complexheatmap
16 months ago by luffy ▴ 130
1
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3
replies
1.9k
views
How to modify labels of complexheatmap
R gene oncoprint complexheatmap
updated 16 months ago by 44k • written 16 months ago by ▴ 130
5
votes
1
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971
views
drug sensitivity prediction
deseq2 oncopredict R drug
updated 17 months ago by ★ 4.3k • written 2.1 years ago by ▴ 130
0
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0
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2.2k
views
Comment: Comment: How to correct unknown Batch effect?
19 months ago by luffy ▴ 130
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1
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2.2k
views
Comment: Comment: How to correct unknown Batch effect?
19 months ago by luffy ▴ 130
4
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5
replies
2.2k
views
How to correct unknown Batch effect?
PCA gene-expression DESeq2 RNA-seq batch-effect
updated 7 months ago by 44k • written 19 months ago by ▴ 130
0
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0
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505
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How to predict drug response or estimate drug sensitivity?
DEGs drugbank IC50 drug R
2.1 years ago by luffy ▴ 130
0
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1
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835
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Comment: Comment: Calculate statistically significance of a small sample size
2.2 years ago by luffy ▴ 130
1
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3
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835
views
Calculate statistically significance of a small sample size
pearson R spearman statistics
updated 2.2 years ago by 10k • written 2.2 years ago by ▴ 130
0
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0
replies
1.5k
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Comment: Comment: Variant identified, What next?
2.2 years ago by luffy ▴ 130
0
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0
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1.5k
views
Comment: Comment: Variant identified, What next?
2.2 years ago by luffy ▴ 130
0
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1
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1.5k
views
Comment: Comment: Variant identified, What next?
2.2 years ago by luffy ▴ 130
4
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7
replies
1.5k
views
Variant identified, What next?
classification variant Exom RNAseq
updated 2.2 years ago by ▴ 430 • written 2.2 years ago by ▴ 130
0
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4
replies
1.4k
views
Extract certain fasta sequnce from multi fasta file
python regex bash fasta
updated 2.3 years ago by ★ 5.1k • written 2.3 years ago by ▴ 130
0
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0
replies
1.2k
views
Comment: Comment: Allele frequency for genes
3.2 years ago by luffy ▴ 130
0
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1
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1.2k
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Comment: Comment: Allele frequency for genes
3.2 years ago by luffy ▴ 130
0
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4
replies
1.2k
views
Allele frequency for genes
frequency gnomAD gene allele
3.2 years ago by luffy ▴ 130
1
vote
1
reply
736
views
Plot a network based on correlation
correlation plot network RNAseq
updated 3.3 years ago by 88k • written 3.3 years ago by ▴ 130
0
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0
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1.3k
views
Comment: Comment: Coordinates long non-coding RNAs
3.6 years ago by luffy ▴ 130
0
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1
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1.3k
views
Comment: Comment: Coordinates long non-coding RNAs
3.6 years ago by luffy ▴ 130
1
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4
replies
1.3k
views
Coordinates long non-coding RNAs
gtf python bedtools rna-seq hg38
3.6 years ago by luffy ▴ 130
0
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1
reply
2.8k
views
Comment: Comment: RNAseq data analysis of pooled data
3.6 years ago by luffy ▴ 130
0
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1
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2.8k
views
Comment: Comment: RNAseq data analysis of pooled data
3.6 years ago by luffy ▴ 130
1
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1
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2.8k
views
Comment: Comment: RNAseq data analysis of pooled data
3.6 years ago by luffy ▴ 130
0
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0
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2.8k
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Comment: Comment: RNAseq data analysis of pooled data
3.6 years ago by luffy ▴ 130
3
votes
4
replies
3.1k
views
Help with CNV calling using ExomeDepth
exomedepth R CNV gCNV exome
updated 3.6 years ago by ▴ 40 • written 4.0 years ago by ▴ 130
7
votes
12
replies
2.8k
views
RNAseq data analysis of pooled data
DESeq2 mapping featurecounts clustering RNA-Seq
updated 3.6 years ago by ★ 2.6k • written 3.6 years ago by ▴ 130
0
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1
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2.8k
views
Comment: Comment: RNAseq data analysis of pooled data
3.6 years ago by luffy ▴ 130
0
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1
reply
823
views
Comment: C: Query regarding variant calling and reporting
3.7 years ago by luffy ▴ 130
0
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3
replies
823
views
Query regarding variant calling and reporting
clinical exome whole exome compound heterozygous
3.7 years ago by luffy ▴ 130
0
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0
replies
2.0k
views
Comment: C: Biological Databases Geographical Distribution
3.9 years ago by luffy ▴ 130
0
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1
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2.0k
views
Comment: C: Biological Databases Geographical Distribution
3.9 years ago by luffy ▴ 130
0
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1
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3.1k
views
Comment: C: Help with CNV calling using ExomeDepth
4.0 years ago by luffy ▴ 130
0
votes
0
replies
924
views
Suggestion for workflow to predict pathogenicity of SNV and INDELs
machine learning python pathogenicity SVM workflow
4.1 years ago by luffy ▴ 130
44 results • Page 1 of 1
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