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6
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1
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19k
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Answer: A: Remove positions that are non-variant in a subset of samples from a vcf file
updated 4.9 years ago by 45k • written 8.7 years ago by ▴ 590
1
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0
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15k
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Answer: A: CNV analysis tool on exome data for NGS
updated 5.3 years ago by 45k • written 11.0 years ago by ▴ 590
1
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0
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4.0k
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Answer: A: Aligner For Mapping Mate Pair (Outies) Data
updated 5.6 years ago by 45k • written 13.1 years ago by ▴ 590
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0
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5.4k
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Comment: C: Interpreting Genome_Structural_Correction Block_Bootstrap.Py
11.1 years ago by Chris Whelan ▴ 590
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0
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9.9k
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Answer: A: How Do I Search A Genome For A Known Motif, And Get An Interval File Of All Inst
11.2 years ago by Chris Whelan ▴ 590
4
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0
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3.9k
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Answer: A: Why Insertion Are Hard To Find By The Alignments Of Reads Than Deletion ?
11.3 years ago by Chris Whelan ▴ 590
2
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0
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33k
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Answer: A: List Of Cloud Genomics Companies
11.4 years ago by Chris Whelan ▴ 590
2
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0
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6.5k
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Answer: A: Tool Or Technique To Find Co-Occuring Motifs Within Genomic Intervals That Corr
11.6 years ago by Chris Whelan ▴ 590
2
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0
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2.4k
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Answer: A: Mapping Applications On Hadoop Cluster
11.6 years ago by Chris Whelan ▴ 590
0
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0
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7.4k
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Comment: C: Publicly Available Pipeline For Analysis Of Whole Genome Bisulfite Sequencing Da
11.7 years ago by Chris Whelan ▴ 590
2
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0
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3.0k
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Answer: A: Pybedtools - Intersect Only Certain Feature Types
11.8 years ago by Chris Whelan ▴ 590
0
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0
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3.9k
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Answer: A: Detection Of Copy Number Variation Between Two Groups Using Whole-Genome Ngs Pai
11.9 years ago by Chris Whelan ▴ 590
0
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0
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5.4k
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Comment: C: False Positive Peaks In Chip-Seq - How To Locate Them And How Do They Arise?
11.9 years ago by Chris Whelan ▴ 590
2
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0
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16k
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Answer: A: How To Improve Mapping Quality By Bowtie2 For Paired End Reads Of Illumina [Hi-C
11.9 years ago by Chris Whelan ▴ 590
1
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0
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7.6k
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Answer: A: Illumina Mate Pair Read Duplication Level
11.9 years ago by Chris Whelan ▴ 590
2
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1
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5.4k
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Answer: A: False Positive Peaks In Chip-Seq - How To Locate Them And How Do They Arise?
11.9 years ago by Chris Whelan ▴ 590
7
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6
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6.7k
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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 12.1 years ago by 102k • written 12.9 years ago by ▴ 590
0
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0
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6.7k
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Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
12.1 years ago by Chris Whelan ▴ 590
0
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0
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4.7k
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Answer: A: Open Source Java De Novo Assembly Software
12.1 years ago by Chris Whelan ▴ 590
0
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0
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5.7k
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Comment: C: Peaksplitter Installation
12.2 years ago by Chris Whelan ▴ 590
0
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1
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3.8k
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Answer: A: Peak Calling In Encode Project
12.2 years ago by Chris Whelan ▴ 590
0
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0
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3.2k
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Comment: C: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
12.4 years ago by Chris Whelan ▴ 590
0
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0
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3.2k
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Comment: C: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
12.4 years ago by Chris Whelan ▴ 590
1
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2
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3.2k
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Answer: A: Simulating Sequences From Simulated Svs At Different Cellular Frequencies
12.4 years ago by Chris Whelan ▴ 590
1
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0
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5.6k
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Answer: A: Macs Peaks Caveat ?
12.5 years ago by Chris Whelan ▴ 590
6
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1
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3.6k
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Answer: A: What Type Of Information Does The Data Downloaded From The 1000 Genomes Contain?
12.5 years ago by Chris Whelan ▴ 590
4
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4
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7.0k
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Answer: A: Why Does Chip-Seq Data Have Lots Of Reverse-Complement Pairs Of Reads?
updated 12.6 years ago by 102k • written 13.1 years ago by ▴ 590
0
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0
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6.7k
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Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
12.7 years ago by Chris Whelan ▴ 590
0
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0
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6.7k
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Comment: C: Need Advice On The Correct Usage For The Genome Structure Correction Statistical
12.7 years ago by Chris Whelan ▴ 590
1
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0
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3.5k
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Answer: A: Breakdancer False Positive
13.0 years ago by Chris Whelan ▴ 590
0
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0
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7.0k
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Comment: C: Why Does Chip-Seq Data Have Lots Of Reverse-Complement Pairs Of Reads?
13.1 years ago by Chris Whelan ▴ 590
2
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1
reply
4.7k
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Answer: A: Genomic Distribution Of Peaks
13.9 years ago by Chris Whelan ▴ 590
2
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0
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7.7k
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Answer: A: Structural Variation; Discordant Pairs?
14.0 years ago by Chris Whelan ▴ 590
4
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0
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70k
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Answer: Answer: What Tools/Libraries Do You Use To Visualize Genomic Feature Data?
updated 17 months ago by 45k • written 14.2 years ago by ▴ 590
1
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0
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29k
views
Comment: C: How Many Bytes Is A Complete Human Genome??
14.2 years ago by Chris Whelan ▴ 590
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