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comments
4
votes
4
replies
6.6k
views
How To Prepare Gatk .Vcf Files Output For Annovar ?
variant
calling
gatk
annovar
vcf
updated 2.4 years ago by
Ram
44k • written 11.4 years ago by
newDNASeqer
▴ 790
7
votes
4
replies
6.7k
views
In Rna-Seq Data, How To Separate Intronic, Exonic, Non-Coding, Snornas ?
rna
updated 3.9 years ago by
Biostar
20 • written 10.7 years ago by
newDNASeqer
▴ 790
2
votes
5
replies
11k
views
What Agilent Interval Files (.Bed) Should I Use For Exome Variant Calling With Gatk?
bed
agilent
gatk
updated 4.8 years ago by
Karma
▴ 310 • written 11.0 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
4.7k
views
Comment:
C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
updated 4.9 years ago by
Ram
44k • written 10.5 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
4.7k
views
Comment:
C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
updated 4.9 years ago by
Ram
44k • written 10.6 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
6.7k
views
Comment:
C: In Rna-Seq Data, How To Separate Intronic, Exonic, Non-Coding, Snornas ?
updated 5.1 years ago by
Ram
44k • written 10.7 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
11k
views
Comment:
C: Paired-End Reads Alignment For Variant Calling ?
updated 5.1 years ago by
Ram
44k • written 11.4 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
3.9k
views
Tophat Error: It Tries To Execute Lines In Fastq Files
tophat
bowtie
error
updated 5.2 years ago by
Biostar
20 • written 11.3 years ago by
newDNASeqer
▴ 790
0
votes
4
replies
4.0k
views
Tophat Error - What Does This Mean?
tophat
error
bowtie
updated 5.7 years ago by
Biostar
20 • written 11.3 years ago by
newDNASeqer
▴ 790
2
votes
7
replies
9.2k
views
How To Filter Vcf By Coverage?
vcf
coverage
updated 7.4 years ago by
aadeokar
• 0 • written 10.7 years ago by
newDNASeqer
▴ 790
4
votes
11
replies
4.7k
views
How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
subclone
cancer
heterogeneity
updated 3.2 years ago by
Ram
44k • written 10.6 years ago by
newDNASeqer
▴ 790
28
votes
13
replies
17k
views
10 follow
Gatk - Haplotypecaller Is So Slow, What Is Faster And As Good?
gatk
updated 8.2 years ago by
daniel
▴ 30 • written 11.3 years ago by
newDNASeqer
▴ 790
31
votes
19
replies
35k
views
12 follow
Trimming Adapters
adaptor
hiseq
updated 9.0 years ago by
Shicheng Guo
★ 9.5k • written 11.4 years ago by
newDNASeqer
▴ 790
6
votes
2
replies
5.4k
views
annotating MAF files
MAF
annotation
updated 3.1 years ago by
Ram
44k • written 10.4 years ago by
newDNASeqer
▴ 790
2
votes
3
replies
4.3k
views
Inferring zygosity information from MAF
MAF
updated 3.0 years ago by
Ram
44k • written 10.4 years ago by
newDNASeqer
▴ 790
0
votes
0
replies
4.1k
views
Comment:
Comment: Dissecting number of forward/reverse reads from GATK output
updated 3.0 years ago by
Ram
44k • written 10.4 years ago by
newDNASeqer
▴ 790
2
votes
3
replies
4.1k
views
Dissecting number of forward/reverse reads from GATK output
reads
gatk
updated 3.0 years ago by
Ram
44k • written 10.4 years ago by
newDNASeqer
▴ 790
5
votes
2
replies
3.7k
views
Downloadable database for human pathways and the associated genes
pathway
database
updated 3.1 years ago by
Ram
44k • written 10.5 years ago by
newDNASeqer
▴ 790
4
votes
3
replies
5.3k
views
How To Convert Hg19_Known_Gene From Text Format To Gtf Or Bed?
hg19
bed
format
conversion
gtf
updated 10.5 years ago by
Kamil
★ 2.3k • written 11.3 years ago by
newDNASeqer
▴ 790
3
votes
5
replies
7.0k
views
What is ref sequence name in BAM file header ?
cn.mops
cnv
updated 3.2 years ago by
Ram
44k • written 10.5 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
4.7k
views
Comment:
C: How to make this kind of 3-D plotting for cancer subclones ? (picture attached)
10.6 years ago by
newDNASeqer
▴ 790
3
votes
2
replies
5.5k
views
Tools For Analyzing Copy Number Variation On All-Tumor Exome-Seq Samples
exome
cnv
updated 10.6 years ago by
Ryan D
★ 3.4k • written 10.7 years ago by
newDNASeqer
▴ 790
0
votes
0
replies
9.2k
views
Comment:
C: How To Filter Vcf By Coverage?
10.7 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
3.5k
views
Comment:
C: Visualizing Cancer Heterogeneity Results From Ngs Data
10.7 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
3.5k
views
Comment:
C: Visualizing Cancer Heterogeneity Results From Ngs Data
10.7 years ago by
newDNASeqer
▴ 790
2
votes
6
replies
3.5k
views
Visualizing Cancer Heterogeneity Results From Ngs Data
cancer
visualization
ngs
updated 10.7 years ago by
Chris Miller
22k • written 10.7 years ago by
newDNASeqer
▴ 790
0
votes
0
replies
9.1k
views
Comment:
C: Search A Dna Sequence Motif In Bam File?
10.7 years ago by
newDNASeqer
▴ 790
3
votes
2
replies
9.1k
views
Search A Dna Sequence Motif In Bam File?
motif
dna
bam
updated 10.7 years ago by
JC
13k • written 10.7 years ago by
newDNASeqer
▴ 790
7
votes
4
replies
6.8k
views
Practice Of Filtering Vcf Files (From Gatk)
filter
vcf
gatk
updated 10.8 years ago by
donfreed
★ 1.6k • written 10.8 years ago by
newDNASeqer
▴ 790
2
votes
1
reply
9.5k
views
How To Create A .Bed File With A Few Candidate Genes?
gene
updated 10.8 years ago by
DG
7.3k • written 10.8 years ago by
newDNASeqer
▴ 790
5
votes
5
replies
7.2k
views
How Do You Usually Filter Variant Calling Results?
filter
updated 10.9 years ago by
Alex Paciorkowski
3.5k • written 10.9 years ago by
newDNASeqer
▴ 790
1
vote
2
replies
2.7k
views
Large Data Set Analysis With Cuffdiff
cuffdiff
rnaseq
updated 2.7 years ago by
Ram
44k • written 10.9 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
2.5k
views
How To Calculate What Gene Expression Is Significant In Cuffdiff
cuffdiff
11.1 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
2.5k
views
How To Merge Cuffdiff (Gene_Exp.Diff) Results From Two Batches Or Rnaseq Data?
cuffdiff
cuffmerge
updated 11.1 years ago by
seidel
11k • written 11.1 years ago by
newDNASeqer
▴ 790
1
vote
2
replies
3.7k
views
Cuffdiff Error With Mouse Mm9 Genome Reference
cuffdiff
updated 11.1 years ago by
Devon Ryan
104k • written 11.1 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
2.7k
views
Cuffmerge Error
cuffmerge
updated 11.1 years ago by
Devon Ryan
104k • written 11.1 years ago by
newDNASeqer
▴ 790
3
votes
1
reply
4.3k
views
Qscript Example For Pipelining Gatk With Queue
gatk
updated 11.2 years ago by
Johan
▴ 890 • written 11.2 years ago by
newDNASeqer
▴ 790
1
vote
2
replies
2.2k
views
Tophat: Option --Bowtie Not A Unique Prefix
tophat
bowtie
updated 11.2 years ago by
jeales
▴ 130 • written 11.2 years ago by
newDNASeqer
▴ 790
0
votes
0
replies
5.0k
views
Comment:
Comment: Tophat - Bowtie 1: Index Error? What'S Wrong?
updated 3.1 years ago by
Ram
44k • written 11.2 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
5.0k
views
Comment:
Comment: Tophat - Bowtie 1: Index Error? What'S Wrong?
updated 3.1 years ago by
Ram
44k • written 11.2 years ago by
newDNASeqer
▴ 790
1
vote
5
replies
5.0k
views
Tophat - Bowtie 1: Index Error? What'S Wrong?
bowtie
updated 3.1 years ago by
Ram
44k • written 11.2 years ago by
newDNASeqer
▴ 790
2
votes
5
replies
4.5k
views
How To Merge Cuffdiff Results To Make A Big Table?
cuffdiff
updated 11.2 years ago by
seidel
11k • written 11.2 years ago by
newDNASeqer
▴ 790
103
votes
9
replies
133k
views
11 follow
How To Merge Two Fastq.Gz Files?
merge
fastq
updated 2.6 years ago by
henry-keen
▴ 40 • written 11.2 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
4.5k
views
Comment:
C: How To Merge Cuffdiff Results To Make A Big Table?
11.2 years ago by
newDNASeqer
▴ 790
0
votes
1
reply
4.0k
views
Comment:
C: Tophat Error - What Does This Mean?
11.3 years ago by
newDNASeqer
▴ 790
0
votes
0
replies
4.4k
views
Comment:
C: Help Needed With Annovar - Csv Summary
11.3 years ago by
newDNASeqer
▴ 790
3
votes
2
replies
4.4k
views
Help Needed With Annovar - Csv Summary
annovar
vcf
updated 11.3 years ago by
Alex Paciorkowski
3.5k • written 11.3 years ago by
newDNASeqer
▴ 790
5
votes
2
replies
3.2k
views
Why # Of Reads From Accepted_Hits.Bam + Unmapped.Bam > # Of Reads In Fastq File?
tophat
fastq
reads
updated 11.3 years ago by
S_Z
▴ 30 • written 11.3 years ago by
newDNASeqer
▴ 790
19
votes
16
replies
11k
views
13 follow
How To Split Reads For Different Flowcell Lanes In Fastq Files?
split
reads
updated 6 weeks ago by
alba
• 0 • written 11.3 years ago by
newDNASeqer
▴ 790
17
votes
6
replies
13k
views
Vcf File --> Gene/Protein Mutation Information
vcf
mutation
annovar
updated 11.3 years ago by
Alex Paciorkowski
3.5k • written 11.4 years ago by
newDNASeqer
▴ 790
67 results • Page
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