Profile Posts Awards
Show
all questions tools blogs news tutorials forum answers comments
4
votes
1
reply
19k
views
Answer: A: Remove positions that are non-variant in a subset of samples from a vcf file
updated 4.6 years ago by 44k • written 8.4 years ago by ▴ 570
1
vote
0
replies
14k
views
Answer: A: CNV analysis tool on exome data for NGS
updated 5.0 years ago by 44k • written 10.7 years ago by ▴ 570
1
vote
0
replies
3.9k
views
Answer: A: Aligner For Mapping Mate Pair (Outies) Data
updated 5.3 years ago by 44k • written 12.8 years ago by ▴ 570
0
votes
0
replies
4.7k
views
Comment: C: Interpreting Genome_Structural_Correction Block_Bootstrap.Py
10.8 years ago by Chris Whelan ▴ 570
0
votes
0
replies
9.7k
views
Answer: A: How Do I Search A Genome For A Known Motif, And Get An Interval File Of All Inst
10.9 years ago by Chris Whelan ▴ 570
4
votes
0
replies
3.7k
views
Answer: A: Why Insertion Are Hard To Find By The Alignments Of Reads Than Deletion ?
11.0 years ago by Chris Whelan ▴ 570
2
votes
0
replies
32k
views
Answer: A: List Of Cloud Genomics Companies
11.1 years ago by Chris Whelan ▴ 570
2
votes
0
replies
6.3k
views
Answer: A: Tool Or Technique To Find Co-Occuring Motifs Within Genomic Intervals That Corr
11.2 years ago by Chris Whelan ▴ 570
2
votes
0
replies
2.3k
views
Answer: A: Mapping Applications On Hadoop Cluster
11.3 years ago by Chris Whelan ▴ 570
0
votes
0
replies
7.2k
views
Comment: C: Publicly Available Pipeline For Analysis Of Whole Genome Bisulfite Sequencing Da
11.4 years ago by Chris Whelan ▴ 570
2
votes
0
replies
2.9k
views
Answer: A: Pybedtools - Intersect Only Certain Feature Types
11.5 years ago by Chris Whelan ▴ 570
0
votes
0
replies
3.8k
views
Answer: A: Detection Of Copy Number Variation Between Two Groups Using Whole-Genome Ngs Pai
11.5 years ago by Chris Whelan ▴ 570
0
votes
0
replies
5.2k
views
Comment: C: False Positive Peaks In Chip-Seq - How To Locate Them And How Do They Arise?
11.5 years ago by Chris Whelan ▴ 570
2
votes
0
replies
16k
views
Answer: A: How To Improve Mapping Quality By Bowtie2 For Paired End Reads Of Illumina [Hi-C
11.5 years ago by Chris Whelan ▴ 570
1
vote
0
replies
7.2k
views
Answer: A: Illumina Mate Pair Read Duplication Level
11.5 years ago by Chris Whelan ▴ 570
2
votes
1
reply
5.2k
views
Answer: A: False Positive Peaks In Chip-Seq - How To Locate Them And How Do They Arise?
11.6 years ago by Chris Whelan ▴ 570
7
votes
6
replies
6.5k
views
Need Advice On The Correct Usage For The Genome Structure Correction Statistical Software From The Encode Project
statistics enrichment encode
updated 11.8 years ago by 102k • written 12.6 years ago by ▴ 570
0
votes
0
replies
6.5k
views
Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
11.8 years ago by Chris Whelan ▴ 570
0
votes
0
replies
4.5k
views
Answer: A: Open Source Java De Novo Assembly Software
11.8 years ago by Chris Whelan ▴ 570
0
votes
0
replies
5.6k
views
Comment: C: Peaksplitter Installation
11.9 years ago by Chris Whelan ▴ 570
0
votes
1
reply
3.7k
views
Answer: A: Peak Calling In Encode Project
11.9 years ago by Chris Whelan ▴ 570
0
votes
0
replies
3.0k
views
Comment: C: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
12.1 years ago by Chris Whelan ▴ 570
0
votes
0
replies
3.0k
views
Comment: C: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
12.1 years ago by Chris Whelan ▴ 570
1
vote
2
replies
3.0k
views
Answer: A: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
12.1 years ago by Chris Whelan ▴ 570
1
vote
0
replies
5.3k
views
Answer: A: Macs Peaks Caveat ?
12.2 years ago by Chris Whelan ▴ 570
6
votes
1
reply
3.5k
views
Answer: A: What Type Of Information Does The Data Downloaded From The 1000 Genomes Contain?
12.2 years ago by Chris Whelan ▴ 570
4
votes
4
replies
6.8k
views
Answer: A: Why Does Chip-Seq Data Have Lots Of Reverse-Complement Pairs Of Reads?
updated 12.3 years ago by 102k • written 12.8 years ago by ▴ 570
0
votes
0
replies
6.5k
views
Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
12.4 years ago by Chris Whelan ▴ 570
0
votes
0
replies
6.5k
views
Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
12.4 years ago by Chris Whelan ▴ 570
1
vote
0
replies
3.4k
views
Answer: A: Breakdancer False Positive
12.7 years ago by Chris Whelan ▴ 570
0
votes
0
replies
6.8k
views
Comment: C: Why Does Chip-Seq Data Have Lots Of Reverse-Complement Pairs Of Reads?
12.8 years ago by Chris Whelan ▴ 570
2
votes
1
reply
4.6k
views
Answer: A: Genomic Distribution Of Peaks
13.6 years ago by Chris Whelan ▴ 570
2
votes
0
replies
7.6k
views
Answer: A: Structural Variation; Discordant Pairs?
13.7 years ago by Chris Whelan ▴ 570
4
votes
0
replies
68k
views
Answer: Answer: What Tools/Libraries Do You Use To Visualize Genomic Feature Data?
updated 13 months ago by 44k • written 13.9 years ago by ▴ 570
1
vote
0
replies
28k
views
Comment: C: How Many Bytes Is A Complete Human Genome??
13.9 years ago by Chris Whelan ▴ 570
35 results • Page 1 of 1
Content Search
Users
Tags
Badges
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6