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newDNASeqer
newDNASeqer
Reputation:
800
Joined:
13.1 years ago
Last seen:
12.1 years ago
Location:
United States

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Latest posts by user
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Comment: Comment: Dissecting number of forward/reverse reads from GATK output
updated by Ram Ram • written by newDNASeqer newDNASeqer
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3 replies
4.8K views
Dissecting number of forward/reverse reads from GATK output
reads gatk
updated by Ram Ram • written by newDNASeqer newDNASeqer
1 vote
3 replies
5.2K views
Inferring zygosity information from MAF
maf
updated by Ram Ram • written by newDNASeqer newDNASeqer
2 votes
2 replies
6.4K views
annotating MAF files
maf annotation
updated by Ram Ram • written by newDNASeqer newDNASeqer
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2 replies
4.3K views
Downloadable database for human pathways and the associated genes
pathway database
updated by Ram Ram • written by newDNASeqer newDNASeqer
1 vote
5 replies
8.1K views
What is ref sequence name in BAM file header ?
cn.mops cnv
updated by Ram Ram • written by newDNASeqer newDNASeqer
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1 reply
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Comment: C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
updated by Ram Ram • written by newDNASeqer newDNASeqer
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1 reply
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Comment: C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
updated by Ram Ram • written by newDNASeqer newDNASeqer
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1 reply
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Comment: C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
written by newDNASeqer newDNASeqer
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11 replies
6.4K views
How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
subclone cancer heterogeneity
updated by Ram Ram • written by newDNASeqer newDNASeqer
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1 reply
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Comment: C: In Rna-Seq Data, How To Separate Intronic, Exonic, Non-Coding, Snornas ?
updated by Ram Ram • written by newDNASeqer newDNASeqer
1 vote
4 replies
7.6K views
In Rna-Seq Data, How To Separate Intronic, Exonic, Non-Coding, Snornas ?
rna
updated by Biostar Biostar • written by newDNASeqer newDNASeqer
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Comment: C: How To Filter Vcf By Coverage?
written by newDNASeqer newDNASeqer
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7 replies
10K views
How To Filter Vcf By Coverage?
vcf coverage
updated by aadeokar • aadeokar • written by newDNASeqer newDNASeqer
3 votes
2 replies
6.2K views
Tools For Analyzing Copy Number Variation On All-Tumor Exome-Seq Samples
exome cnv
updated by Ryan D Ryan D • written by newDNASeqer newDNASeqer
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1 reply
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Comment: C: Visualizing Cancer Heterogeneity Results From Ngs Data
written by newDNASeqer newDNASeqer
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1 reply
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Comment: C: Visualizing Cancer Heterogeneity Results From Ngs Data
written by newDNASeqer newDNASeqer
1 vote
6 replies
4.4K views
Visualizing Cancer Heterogeneity Results From Ngs Data
cancer visualization ngs
updated by Chris Miller Chris Miller • written by newDNASeqer newDNASeqer
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Comment: C: Search A Dna Sequence Motif In Bam File?
written by newDNASeqer newDNASeqer
1 vote
2 replies
10K views
Search A Dna Sequence Motif In Bam File?
motif dna bam
updated by JC JC • written by newDNASeqer newDNASeqer
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