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8.2k
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Answer:
Answer: How to compute physical per-base coverage from WGS paired-end reads?
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Fidel
★ 2.0k
0
votes
1
reply
4.8k
views
Comment:
Comment: Application of Hi-C
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Fidel
★ 2.0k
0
votes
0
replies
8.2k
views
Comment:
Comment: How to compute physical per-base coverage from WGS paired-end reads?
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Fidel
★ 2.0k
1
vote
1
reply
2.0k
views
Answer:
Answer: What are the steps to follow to extract a promoter region starting from illumina
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Fidel
★ 2.0k
0
votes
1
reply
4.8k
views
Comment:
Comment: Application of Hi-C
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Fidel
★ 2.0k
2
votes
1
reply
4.8k
views
Answer:
Answer: Application of Hi-C
updated 2.6 years ago by
Ram
44k • written 9.8 years ago by
Fidel
★ 2.0k
0
votes
0
replies
4.3k
views
Comment:
C: Scan a large genome for the ocurrence of a single sequence motif?
9.8 years ago by
Fidel
★ 2.0k
0
votes
0
replies
11k
views
Comment:
C: Normalising ChIP-seq data to RPM using a 1 or 2 count for paired-end data?
9.9 years ago by
Fidel
★ 2.0k
0
votes
0
replies
11k
views
Comment:
Comment: Normalising ChIP-seq data to RPM using a 1 or 2 count for paired-end data?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
11k
views
Comment:
C: Normalising ChIP-seq data to RPM using a 1 or 2 count for paired-end data?
9.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
11k
views
Comment:
Comment: Normalising ChIP-seq data to RPM using a 1 or 2 count for paired-end data?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
8
votes
1
reply
11k
views
Answer:
Answer: Normalising ChIP-seq data to RPM using a 1 or 2 count for paired-end data?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
4.3k
views
Comment:
Comment: Scan a large genome for the ocurrence of a single sequence motif?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
4.3k
views
Comment:
Comment: Scan a large genome for the ocurrence of a single sequence motif?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
1
vote
1
reply
3.4k
views
Comment:
Comment: Metaseq: Average ChIP-seq signal over promoters error
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
2.0k
views
Comment:
Comment: Analysis for Unknwon motifs obtained from Meme or Dream.
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
1
vote
2
replies
4.3k
views
Comment:
Comment: Scan a large genome for the ocurrence of a single sequence motif?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
1
vote
1
reply
4.3k
views
Answer:
Answer: Scan a large genome for the ocurrence of a single sequence motif?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
10k
views
Answer:
Answer: How do I view the height / distribution of ChIP-seq peaks?
updated 2.7 years ago by
Ram
44k • written 9.9 years ago by
Fidel
★ 2.0k
4
votes
1
reply
16k
views
Answer:
A: Best Way To Get Truly Unique Reads In Bowtie/Sam?
updated 10.7 years ago by
seidel
11k • written 12.1 years ago by
Fidel
★ 2.0k
2
votes
0
replies
3.6k
views
Answer:
A: Count The Coverage Rate Of A Bacterial Genome'S Bam File
10.7 years ago by
Fidel
★ 2.0k
7
votes
0
replies
12k
views
Answer:
A: How To Plot Read Coverage Over Many Different Genomic Regions?
10.7 years ago by
Fidel
★ 2.0k
1
vote
0
replies
12k
views
Answer:
A: Emule "Samtools View" Using Pysam
10.9 years ago by
Fidel
★ 2.0k
5
votes
1
reply
14k
views
Answer:
A: Chipseq Wig File With The Input Subtracted From Chip Sample
11.0 years ago by
Fidel
★ 2.0k
5
votes
8
replies
13k
views
How To Read A Bigwig File Using Python
python
bigwig
updated 11.2 years ago by
tszn1984
▴ 100 • written 12.7 years ago by
Fidel
★ 2.0k
1
vote
0
replies
3.7k
views
Answer:
A: 'Potential Rna-Dna Binding Site In Alu Repeat', Or 'Why Should I Allow Multiple
11.4 years ago by
Fidel
★ 2.0k
11
votes
0
replies
42k
views
Answer:
A: Is It Possible To Get Fragment Length, Read Length And Number Of Fragments From
11.5 years ago by
Fidel
★ 2.0k
17
votes
3
replies
16k
views
Is There Any Advantage Of Paired End Sequencing For Chip-Seq?
paired-end
chip-seq
updated 11.7 years ago by
Ian
6.1k • written 11.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
4.3k
views
Answer:
A: Identification Of Protein Complexes In A List Of Proteins
11.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
12k
views
Comment:
C: How To Plot Read Coverage Over Many Different Genomic Regions?
11.9 years ago by
Fidel
★ 2.0k
0
votes
1
reply
12k
views
Answer:
A: How To Plot Read Coverage Over Many Different Genomic Regions?
11.9 years ago by
Fidel
★ 2.0k
2
votes
1
reply
2.1k
views
Answer:
A: Dna-Seq Multiple Mapped Tags
updated 12.0 years ago by
Istvan Albert
102k • written 12.0 years ago by
Fidel
★ 2.0k
0
votes
1
reply
16k
views
Comment:
C: Best Way To Get Truly Unique Reads In Bowtie/Sam?
12.1 years ago by
Fidel
★ 2.0k
5
votes
0
replies
3.1k
views
Answer:
A: Visualization Of Read Count On Genome
12.1 years ago by
Fidel
★ 2.0k
0
votes
0
replies
19k
views
Comment:
C: Bioinformatics Training On Next-Generation Sequencing Data
12.1 years ago by
Fidel
★ 2.0k
2
votes
0
replies
5.0k
views
Answer:
A: Differential Open Chromatin Locations From Dnase-Seq Data
12.1 years ago by
Fidel
★ 2.0k
0
votes
0
replies
2.7k
views
Answer:
A: Create Image From Mapping Region
12.2 years ago by
Fidel
★ 2.0k
0
votes
0
replies
3.7k
views
Comment:
C: Bowtie Inaccuracy Limit
12.5 years ago by
Fidel
★ 2.0k
0
votes
1
reply
6.6k
views
Comment:
C: Peak Calling Biasing!!! [Macs14]
12.5 years ago by
Fidel
★ 2.0k
0
votes
1
reply
3.2k
views
Comment:
C: Is The Example In The Sam Format Specification Documentation Incorrect?
12.5 years ago by
Fidel
★ 2.0k
0
votes
0
replies
3.1k
views
Answer:
A: Convert Un-Indexed Sam File To Wig File
12.6 years ago by
Fidel
★ 2.0k
1
vote
1
reply
7.7k
views
Answer:
A: Building A Webpage For Accessing Rna-Seq Expression Data
12.7 years ago by
Fidel
★ 2.0k
5
votes
2
replies
9.5k
views
Answer:
A: Why Does Macs Use A Genome Size Of 2.7 Billion Instead Of 3 Billion For Human?
12.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
9.5k
views
Comment:
C: Why Does Macs Use A Genome Size Of 2.7 Billion Instead Of 3 Billion For Human?
12.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
13k
views
Comment:
C: How To Read A Bigwig File Using Python
12.7 years ago by
Fidel
★ 2.0k
1
vote
0
replies
13k
views
Comment:
C: How To Read A Bigwig File Using Python
12.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
3.4k
views
Comment:
C: Pharmgkb: Obtain A List Of Vip Genes And List All Linked Drugs To Them
12.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
3.4k
views
Comment:
C: Pharmgkb: Obtain A List Of Vip Genes And List All Linked Drugs To Them
12.7 years ago by
Fidel
★ 2.0k
7
votes
0
replies
7.3k
views
Answer:
A: Calculating The Depth/Level Of Shared Gene Ontology (Go) Terms Between Protein P
12.7 years ago by
Fidel
★ 2.0k
0
votes
0
replies
4.5k
views
Comment:
C: Gc Content In Mate Pairs / Pair-End
12.8 years ago by
Fidel
★ 2.0k
159 results • Page
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