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4
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1
reply
17k
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Answer: A: Remove positions that are non-variant in a subset of samples from a vcf file
updated 4.0 years ago by 43k • written 7.7 years ago by ▴ 570
1
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0
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13k
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Answer: A: CNV analysis tool on exome data for NGS
updated 4.3 years ago by 43k • written 10.0 years ago by ▴ 570
1
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0
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3.7k
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Answer: A: Aligner For Mapping Mate Pair (Outies) Data
updated 4.6 years ago by 43k • written 12.1 years ago by ▴ 570
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0
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4.3k
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Comment: C: Interpreting Genome_Structural_Correction Block_Bootstrap.Py
10.1 years ago by Chris Whelan ▴ 570
0
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0
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9.4k
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Answer: A: How Do I Search A Genome For A Known Motif, And Get An Interval File Of All Inst
10.2 years ago by Chris Whelan ▴ 570
4
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0
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3.4k
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Answer: A: Why Insertion Are Hard To Find By The Alignments Of Reads Than Deletion ?
10.3 years ago by Chris Whelan ▴ 570
2
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0
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31k
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Answer: A: List Of Cloud Genomics Companies
10.5 years ago by Chris Whelan ▴ 570
2
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0
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6.1k
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Answer: A: Tool Or Technique To Find Co-Occuring Motifs Within Genomic Intervals That Corr
10.6 years ago by Chris Whelan ▴ 570
2
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0
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2.2k
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Answer: A: Mapping Applications On Hadoop Cluster
10.6 years ago by Chris Whelan ▴ 570
0
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0
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6.9k
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Comment: C: Publicly Available Pipeline For Analysis Of Whole Genome Bisulfite Sequencing Da
10.8 years ago by Chris Whelan ▴ 570
2
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0
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2.8k
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Answer: A: Pybedtools - Intersect Only Certain Feature Types
10.8 years ago by Chris Whelan ▴ 570
0
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0
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3.7k
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Answer: A: Detection Of Copy Number Variation Between Two Groups Using Whole-Genome Ngs Pai
10.9 years ago by Chris Whelan ▴ 570
0
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0
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4.9k
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Comment: C: False Positive Peaks In Chip-Seq - How To Locate Them And How Do They Arise?
10.9 years ago by Chris Whelan ▴ 570
2
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0
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15k
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Answer: A: How To Improve Mapping Quality By Bowtie2 For Paired End Reads Of Illumina [Hi-C
10.9 years ago by Chris Whelan ▴ 570
1
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0
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6.7k
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Answer: A: Illumina Mate Pair Read Duplication Level
10.9 years ago by Chris Whelan ▴ 570
2
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1
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4.9k
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Answer: A: False Positive Peaks In Chip-Seq - How To Locate Them And How Do They Arise?
10.9 years ago by Chris Whelan ▴ 570
7
votes
6
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6.3k
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Need Advice On The Correct Usage For The Genome Structure Correction Statistical Software From The Encode Project
statistics enrichment encode
updated 11.1 years ago by 100k • written 11.9 years ago by ▴ 570
0
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0
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6.3k
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Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
11.1 years ago by Chris Whelan ▴ 570
0
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0
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4.3k
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Answer: A: Open Source Java De Novo Assembly Software
11.2 years ago by Chris Whelan ▴ 570
0
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0
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5.4k
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Comment: C: Peaksplitter Installation
11.2 years ago by Chris Whelan ▴ 570
0
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1
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3.5k
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Answer: A: Peak Calling In Encode Project
11.2 years ago by Chris Whelan ▴ 570
0
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0
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2.8k
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Comment: C: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
11.4 years ago by Chris Whelan ▴ 570
0
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0
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2.8k
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Comment: C: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
11.4 years ago by Chris Whelan ▴ 570
1
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2
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2.8k
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Answer: A: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
11.4 years ago by Chris Whelan ▴ 570
1
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0
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5.0k
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Answer: A: Macs Peaks Caveat ?
11.5 years ago by Chris Whelan ▴ 570
6
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1
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3.3k
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Answer: A: What Type Of Information Does The Data Downloaded From The 1000 Genomes Contain?
11.5 years ago by Chris Whelan ▴ 570
4
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4
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6.4k
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Answer: A: Why Does Chip-Seq Data Have Lots Of Reverse-Complement Pairs Of Reads?
updated 11.6 years ago by 100k • written 12.1 years ago by ▴ 570
0
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0
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6.3k
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Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
11.7 years ago by Chris Whelan ▴ 570
0
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0
replies
6.3k
views
Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
11.7 years ago by Chris Whelan ▴ 570
1
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0
replies
3.2k
views
Answer: A: Breakdancer False Positive
12.0 years ago by Chris Whelan ▴ 570
0
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0
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6.4k
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Comment: C: Why Does Chip-Seq Data Have Lots Of Reverse-Complement Pairs Of Reads?
12.1 years ago by Chris Whelan ▴ 570
2
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1
reply
4.4k
views
Answer: A: Genomic Distribution Of Peaks
12.9 years ago by Chris Whelan ▴ 570
2
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0
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7.3k
views
Answer: A: Structural Variation; Discordant Pairs?
13.0 years ago by Chris Whelan ▴ 570
4
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0
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64k
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Answer: Answer: What Tools/Libraries Do You Use To Visualize Genomic Feature Data?
updated 5 months ago by 43k • written 13.2 years ago by ▴ 570
1
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0
replies
26k
views
Comment: C: How Many Bytes Is A Complete Human Genome??
13.2 years ago by Chris Whelan ▴ 570
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