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Comment: Comment: Prediction tools summary - zero values
6 months ago by luffy ▴ 110
1
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0
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612
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Comment: Comment: How to choose the best tool for variant trio analysis
6 months ago by luffy ▴ 110
3
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1
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1.0k
views
Answer: Answer: Prediction tools summary - zero values
6 months ago by luffy ▴ 110
0
votes
1
reply
326
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small RNAseq analysis of non human samples
lncRNA sRNA DEG small-RNA RNA-seq
updated 6 months ago by 43k • written 6 months ago by ▴ 110
1
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0
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836
views
Comment: Comment: identify DEGs across all conditions and per specific conditions
7 months ago by luffy ▴ 110
1
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1
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676
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Comment: Comment: Which function is best for pathway analysis?
7 months ago by luffy ▴ 110
1
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0
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509
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Answer: Answer: How to retrieve LoF and missense variants in WES data?
7 months ago by luffy ▴ 110
1
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0
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577
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Answer: Answer: functional and genome annotation analysis
7 months ago by luffy ▴ 110
0
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0
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942
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Answer: Answer: matching gnomAD allele frequency
8 months ago by luffy ▴ 110
0
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0
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472
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Comment: Comment: Denovo variants
8 months ago by luffy ▴ 110
0
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1
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1.4k
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Comment: Comment: How to modify labels of complexheatmap
9 months ago by luffy ▴ 110
1
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3
replies
1.4k
views
How to modify labels of complexheatmap
R gene oncoprint complexheatmap
updated 9 months ago by 43k • written 9 months ago by ▴ 110
5
votes
1
reply
726
views
drug sensitivity prediction
deseq2 oncopredict R drug
updated 10 months ago by ★ 4.3k • written 18 months ago by ▴ 110
0
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0
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1.5k
views
Comment: Comment: How to correct unknown Batch effect?
12 months ago by luffy ▴ 110
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1
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1.5k
views
Comment: Comment: How to correct unknown Batch effect?
12 months ago by luffy ▴ 110
1
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5
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1.5k
views
How to correct unknown Batch effect?
PCA gene-expression DESeq2 RNA-seq batch-effect
updated 10 days ago by 43k • written 12 months ago by ▴ 110
0
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0
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409
views
How to predict drug response or estimate drug sensitivity?
DEGs drugbank IC50 drug R
18 months ago by luffy ▴ 110
0
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1
reply
682
views
Comment: Comment: Calculate statistically significance of a small sample size
19 months ago by luffy ▴ 110
1
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3
replies
682
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Calculate statistically significance of a small sample size
pearson R spearman statistics
updated 19 months ago by 10k • written 19 months ago by ▴ 110
0
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0
replies
1.2k
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Comment: Comment: Variant identified, What next?
20 months ago by luffy ▴ 110
0
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0
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1.2k
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Comment: Comment: Variant identified, What next?
20 months ago by luffy ▴ 110
0
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1
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1.2k
views
Comment: Comment: Variant identified, What next?
20 months ago by luffy ▴ 110
4
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7
replies
1.2k
views
Variant identified, What next?
classification variant Exom RNAseq
updated 20 months ago by ▴ 390 • written 20 months ago by ▴ 110
0
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4
replies
1.2k
views
Extract certain fasta sequnce from multi fasta file
python regex bash fasta
updated 21 months ago by ★ 5.1k • written 21 months ago by ▴ 110
0
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0
replies
1.0k
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Comment: Comment: Allele frequency for genes
2.6 years ago by luffy ▴ 110
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1
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1.0k
views
Comment: Comment: Allele frequency for genes
2.6 years ago by luffy ▴ 110
0
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4
replies
1.0k
views
Allele frequency for genes
frequency gnomAD gene allele
2.6 years ago by luffy ▴ 110
1
vote
1
reply
665
views
Plot a network based on correlation
correlation plot network RNAseq
updated 2.8 years ago by 87k • written 2.8 years ago by ▴ 110
0
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0
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1.2k
views
Comment: Comment: Coordinates long non-coding RNAs
3.0 years ago by luffy ▴ 110
0
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1
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1.2k
views
Comment: Comment: Coordinates long non-coding RNAs
3.0 years ago by luffy ▴ 110
1
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4
replies
1.2k
views
Coordinates long non-coding RNAs
gtf python bedtools rna-seq hg38
3.0 years ago by luffy ▴ 110
0
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1
reply
2.5k
views
Comment: Comment: RNAseq data analysis of pooled data
3.0 years ago by luffy ▴ 110
0
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1
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2.5k
views
Comment: Comment: RNAseq data analysis of pooled data
3.0 years ago by luffy ▴ 110
1
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1
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2.5k
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Comment: Comment: RNAseq data analysis of pooled data
3.0 years ago by luffy ▴ 110
0
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0
replies
2.5k
views
Comment: Comment: RNAseq data analysis of pooled data
3.0 years ago by luffy ▴ 110
3
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4
replies
2.8k
views
Help with CNV calling using ExomeDepth
exomedepth R CNV gCNV exome
updated 3.0 years ago by ▴ 40 • written 3.4 years ago by ▴ 110
7
votes
12
replies
2.5k
views
RNAseq data analysis of pooled data
DESeq2 mapping featurecounts clustering RNA-Seq
updated 3.0 years ago by ★ 2.6k • written 3.0 years ago by ▴ 110
0
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1
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2.5k
views
Comment: Comment: RNAseq data analysis of pooled data
3.0 years ago by luffy ▴ 110
0
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1
reply
694
views
Comment: C: Query regarding variant calling and reporting
3.1 years ago by luffy ▴ 110
0
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3
replies
694
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Query regarding variant calling and reporting
clinical exome whole exome compound heterozygous
3.1 years ago by luffy ▴ 110
0
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0
replies
1.8k
views
Comment: C: Biological Databases Geographical Distribution
3.4 years ago by luffy ▴ 110
0
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1
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1.8k
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Comment: C: Biological Databases Geographical Distribution
3.4 years ago by luffy ▴ 110
0
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1
reply
2.8k
views
Comment: C: Help with CNV calling using ExomeDepth
3.4 years ago by luffy ▴ 110
0
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0
replies
844
views
Suggestion for workflow to predict pathogenicity of SNV and INDELs
machine learning python pathogenicity SVM workflow
3.5 years ago by luffy ▴ 110
44 results • Page 1 of 1
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