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511
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Comment:
Comment: complexity in sn/scRNASeq explanation
21 months ago by
Sharon
▴ 600
0
votes
0
replies
818
views
Comment:
C: Get Germline variants from Biomart
3.7 years ago by
Sharon
▴ 600
0
votes
0
replies
818
views
Comment:
C: Get Germline variants from Biomart
3.7 years ago by
Sharon
▴ 600
2
votes
1
reply
3.3k
views
Comment:
C: GT 2/3, or 3/3 or 2/2 in vcf
3.9 years ago by
Sharon
▴ 600
0
votes
0
replies
7.3k
views
Comment:
C: How to fix this strand flips for Michigan Imputation Server?
4.9 years ago by
Sharon
▴ 600
0
votes
0
replies
11k
views
Comment:
C: Relatedness vs relatedness2 from vcftools give different results
4.9 years ago by
Sharon
▴ 600
0
votes
1
reply
4.2k
views
Comment:
C: Annovar for mouse buildver and downdb?
4.9 years ago by
Sharon
▴ 600
0
votes
1
reply
7.3k
views
Comment:
C: How to fix this strand flips for Michigan Imputation Server?
5.3 years ago by
Sharon
▴ 600
0
votes
1
reply
7.3k
views
Comment:
C: How to fix this strand flips for Michigan Imputation Server?
5.3 years ago by
Sharon
▴ 600
0
votes
1
reply
7.3k
views
Comment:
C: How to fix this strand flips for Michigan Imputation Server?
5.4 years ago by
Sharon
▴ 600
1
vote
0
replies
2.2k
views
Comment:
C: How to remove duplicate sites and inconsistent sites from a VCF?
5.4 years ago by
Sharon
▴ 600
0
votes
0
replies
1.4k
views
Comment:
C: Validate interesting gene from a burden test and association studies (SkatO, etc
5.7 years ago by
Sharon
▴ 600
1
vote
0
replies
4.6k
views
Comment:
C: How tximport work with gencode transcripts?
5.8 years ago by
Sharon
▴ 600
0
votes
1
reply
4.6k
views
Comment:
C: How tximport work with gencode transcripts?
5.8 years ago by
Sharon
▴ 600
0
votes
0
replies
1.9k
views
Comment:
C: How to present/evaluate RNAseq deconvolution results?
5.8 years ago by
Sharon
▴ 600
1
vote
1
reply
1.5k
views
Comment:
C: Coverage in whole genome sequencing
5.9 years ago by
Sharon
▴ 600
0
votes
0
replies
1.3k
views
Comment:
C: Genes' length to get RPKM if features count is not used?
5.9 years ago by
Sharon
▴ 600
0
votes
0
replies
1.7k
views
Comment:
C: Help explain novel lncRNA results
5.9 years ago by
Sharon
▴ 600
0
votes
0
replies
1.7k
views
Comment:
C: Help explain novel lncRNA results
5.9 years ago by
Sharon
▴ 600
0
votes
1
reply
1.7k
views
Comment:
C: Help explain novel lncRNA results
5.9 years ago by
Sharon
▴ 600
0
votes
0
replies
4.7k
views
Comment:
C: How can I convert from bed to bed12 format?
5.9 years ago by
Sharon
▴ 600
0
votes
1
reply
4.7k
views
Comment:
C: How can I convert from bed to bed12 format?
5.9 years ago by
Sharon
▴ 600
0
votes
1
reply
4.7k
views
Comment:
C: How can I convert from bed to bed12 format?
5.9 years ago by
Sharon
▴ 600
1
vote
0
replies
1.6k
views
Comment:
C: Variant with AD 14,3 is heterozygote?
5.9 years ago by
Sharon
▴ 600
0
votes
1
reply
1.6k
views
Comment:
C: Variant with AD 14,3 is heterozygote?
5.9 years ago by
Sharon
▴ 600
1
vote
0
replies
1.6k
views
Comment:
C: Variant with AD 14,3 is heterozygote?
5.9 years ago by
Sharon
▴ 600
0
votes
0
replies
1.5k
views
Comment:
C: cufflinks missing some annotations?
5.9 years ago by
Sharon
▴ 600
0
votes
0
replies
1.7k
views
Comment:
C: Builiding reference for annovar based on build37.1?
5.9 years ago by
Sharon
▴ 600
0
votes
1
reply
1.7k
views
Comment:
C: Builiding reference for annovar based on build37.1?
5.9 years ago by
Sharon
▴ 600
1
vote
0
replies
2.6k
views
Comment:
C: problem plotting heatmap for pathways?
6.0 years ago by
Sharon
▴ 600
1
vote
1
reply
2.6k
views
Comment:
C: problem plotting heatmap for pathways?
6.0 years ago by
Sharon
▴ 600
0
votes
1
reply
2.6k
views
Comment:
C: problem plotting heatmap for pathways?
6.0 years ago by
Sharon
▴ 600
0
votes
1
reply
2.6k
views
Comment:
C: problem plotting heatmap for pathways?
6.0 years ago by
Sharon
▴ 600
0
votes
0
replies
2.5k
views
Comment:
C: How to fix mismatch between snp file and reference?
6.0 years ago by
Sharon
▴ 600
1
vote
0
replies
1.4k
views
Comment:
C: Should we discard a variant if it pass many filters and fails one?
6.0 years ago by
Sharon
▴ 600
0
votes
0
replies
1.4k
views
Comment:
C: Should we discard a variant if it pass many filters and fails one?
6.0 years ago by
Sharon
▴ 600
0
votes
0
replies
2.5k
views
Comment:
C: How to fix mismatch between snp file and reference?
6.0 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: How to fix mismatch between snp file and reference?
6.0 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: How to fix mismatch between snp file and reference?
6.0 years ago by
Sharon
▴ 600
0
votes
1
reply
1.0k
views
Comment:
C: Why FS is low when reads aligned from strand seem biased?
6.0 years ago by
Sharon
▴ 600
1
vote
0
replies
1.3k
views
Comment:
C: Is is a possible mosaic / effect of downsampling?
6.1 years ago by
Sharon
▴ 600
0
votes
1
reply
1.3k
views
Comment:
C: Is is a possible mosaic / effect of downsampling?
6.1 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: Is this variant probably an artifact?
6.1 years ago by
Sharon
▴ 600
1
vote
0
replies
2.5k
views
Comment:
C: Is this variant probably an artifact?
6.1 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: Is this variant probably an artifact?
6.1 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: Is this variant probably an artifact?
6.1 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: Is this variant probably an artifact?
6.1 years ago by
Sharon
▴ 600
0
votes
1
reply
2.5k
views
Comment:
C: Is this variant probably an artifact?
6.1 years ago by
Sharon
▴ 600
0
votes
0
replies
1.7k
views
Comment:
C: High Duplication and low coverage RNASeq?
6.1 years ago by
Sharon
▴ 600
0
votes
0
replies
1.7k
views
Comment:
C: High Duplication and low coverage RNASeq?
6.1 years ago by
Sharon
▴ 600
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