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Comment: Comment: complexity in sn/scRNASeq explanation
23 months ago by Sharon ▴ 610
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0
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856
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Comment: C: Get Germline variants from Biomart
3.9 years ago by Sharon ▴ 610
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0
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856
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Comment: C: Get Germline variants from Biomart
3.9 years ago by Sharon ▴ 610
2
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1
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3.5k
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Comment: C: GT 2/3, or 3/3 or 2/2 in vcf
4.0 years ago by Sharon ▴ 610
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0
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7.5k
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Comment: C: How to fix this strand flips for Michigan Imputation Server?
5.0 years ago by Sharon ▴ 610
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11k
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Comment: C: Relatedness vs relatedness2 from vcftools give different results
5.0 years ago by Sharon ▴ 610
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1
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4.4k
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Comment: C: Annovar for mouse buildver and downdb?
5.0 years ago by Sharon ▴ 610
0
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1
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7.5k
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Comment: C: How to fix this strand flips for Michigan Imputation Server?
5.4 years ago by Sharon ▴ 610
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1
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7.5k
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Comment: C: How to fix this strand flips for Michigan Imputation Server?
5.4 years ago by Sharon ▴ 610
0
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1
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7.5k
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Comment: C: How to fix this strand flips for Michigan Imputation Server?
5.5 years ago by Sharon ▴ 610
1
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0
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2.3k
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Comment: C: How to remove duplicate sites and inconsistent sites from a VCF?
5.5 years ago by Sharon ▴ 610
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0
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1.4k
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Comment: C: Validate interesting gene from a burden test and association studies (SkatO, etc
5.8 years ago by Sharon ▴ 610
1
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0
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4.6k
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Comment: C: How tximport work with gencode transcripts?
5.9 years ago by Sharon ▴ 610
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1
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4.6k
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Comment: C: How tximport work with gencode transcripts?
5.9 years ago by Sharon ▴ 610
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0
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1.9k
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Comment: C: How to present/evaluate RNAseq deconvolution results?
5.9 years ago by Sharon ▴ 610
1
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1
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1.6k
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Comment: C: Coverage in whole genome sequencing
6.0 years ago by Sharon ▴ 610
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1.3k
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Comment: C: Genes' length to get RPKM if features count is not used?
6.0 years ago by Sharon ▴ 610
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1.7k
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Comment: C: Help explain novel lncRNA results
6.0 years ago by Sharon ▴ 610
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0
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1.7k
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Comment: C: Help explain novel lncRNA results
6.0 years ago by Sharon ▴ 610
0
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1
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1.7k
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Comment: C: Help explain novel lncRNA results
6.0 years ago by Sharon ▴ 610
0
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0
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4.9k
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Comment: C: How can I convert from bed to bed12 format?
6.0 years ago by Sharon ▴ 610
0
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1
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4.9k
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Comment: C: How can I convert from bed to bed12 format?
6.0 years ago by Sharon ▴ 610
0
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1
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4.9k
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Comment: C: How can I convert from bed to bed12 format?
6.0 years ago by Sharon ▴ 610
1
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0
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1.7k
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Comment: C: Variant with AD 14,3 is heterozygote?
6.0 years ago by Sharon ▴ 610
0
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1
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1.7k
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Comment: C: Variant with AD 14,3 is heterozygote?
6.0 years ago by Sharon ▴ 610
1
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0
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1.7k
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Comment: C: Variant with AD 14,3 is heterozygote?
6.0 years ago by Sharon ▴ 610
0
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0
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1.6k
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Comment: C: cufflinks missing some annotations?
6.0 years ago by Sharon ▴ 610
0
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0
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1.7k
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Comment: C: Builiding reference for annovar based on build37.1?
6.1 years ago by Sharon ▴ 610
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1
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1.7k
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Comment: C: Builiding reference for annovar based on build37.1?
6.1 years ago by Sharon ▴ 610
1
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0
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2.6k
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Comment: C: problem plotting heatmap for pathways?
6.1 years ago by Sharon ▴ 610
1
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1
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2.6k
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Comment: C: problem plotting heatmap for pathways?
6.1 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: problem plotting heatmap for pathways?
6.1 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: problem plotting heatmap for pathways?
6.1 years ago by Sharon ▴ 610
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0
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2.6k
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Comment: C: How to fix mismatch between snp file and reference?
6.1 years ago by Sharon ▴ 610
1
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0
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1.4k
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Comment: C: Should we discard a variant if it pass many filters and fails one?
6.1 years ago by Sharon ▴ 610
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0
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1.4k
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Comment: C: Should we discard a variant if it pass many filters and fails one?
6.1 years ago by Sharon ▴ 610
0
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0
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2.6k
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Comment: C: How to fix mismatch between snp file and reference?
6.1 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: How to fix mismatch between snp file and reference?
6.1 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: How to fix mismatch between snp file and reference?
6.1 years ago by Sharon ▴ 610
0
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1
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1.1k
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Comment: C: Why FS is low when reads aligned from strand seem biased?
6.1 years ago by Sharon ▴ 610
1
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0
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1.3k
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Comment: C: Is is a possible mosaic / effect of downsampling?
6.2 years ago by Sharon ▴ 610
0
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1
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1.3k
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Comment: C: Is is a possible mosaic / effect of downsampling?
6.2 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: Is this variant probably an artifact?
6.2 years ago by Sharon ▴ 610
1
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0
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2.6k
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Comment: C: Is this variant probably an artifact?
6.2 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: Is this variant probably an artifact?
6.2 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: Is this variant probably an artifact?
6.2 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: Is this variant probably an artifact?
6.2 years ago by Sharon ▴ 610
0
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1
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2.6k
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Comment: C: Is this variant probably an artifact?
6.2 years ago by Sharon ▴ 610
0
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0
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1.8k
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Comment: C: High Duplication and low coverage RNASeq?
6.2 years ago by Sharon ▴ 610
0
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0
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1.8k
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Comment: C: High Duplication and low coverage RNASeq?
6.2 years ago by Sharon ▴ 610
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