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Answer: A: txt file to bigwig
5.9 years ago by Dataman ▴ 350
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3.6k
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Comment: C: txt file to bigwig
5.9 years ago by Dataman ▴ 350
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22k
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Comment: C: samtools bedcov vs. bedtools coverage
6.0 years ago by Dataman ▴ 350
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22k
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Comment: C: samtools bedcov vs. bedtools coverage
6.0 years ago by Dataman ▴ 350
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22k
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Comment: C: samtools bedcov vs. bedtools coverage
6.0 years ago by Dataman ▴ 350
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22k
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Comment: C: samtools bedcov vs. bedtools coverage
6.0 years ago by Dataman ▴ 350
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10k
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Comment: C: Get Snp Position From A Python Interface.
6.0 years ago by Dataman ▴ 350
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8.6k
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Answer: A: Gene set enrichment tool for RNA-Seq in Python?
6.0 years ago by Dataman ▴ 350
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1
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3.1k
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Comment: C: what does Num_Probes in a segmentation file refer to?
6.2 years ago by Dataman ▴ 350
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1
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3.1k
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Comment: C: what does Num_Probes in a segmentation file refer to?
6.2 years ago by Dataman ▴ 350
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5
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3.1k
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what does Num_Probes in a segmentation file refer to?
sequencing
updated 6.2 years ago by ★ 2.9k • written 6.2 years ago by ▴ 350
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4.7k
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Comment: C: CNA calculation from Segmentation file
6.2 years ago by Dataman ▴ 350
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15k
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Comment: C: TCGA Segement Mean, GISTIC and CNVs
6.2 years ago by Dataman ▴ 350
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15
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4.9k
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6 follow
What is the best way to make a bam file smaller by removing unwanted information?
next-gen bam sequencing compression
6.3 years ago by Dataman ▴ 350
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4.9k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
6.3 years ago by Dataman ▴ 350
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1
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4.9k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
6.3 years ago by Dataman ▴ 350
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1
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4.9k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
6.3 years ago by Dataman ▴ 350
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9.7k
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Comment: C: Is There Any Reference Exome ?
6.9 years ago by Dataman ▴ 350
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4.1k
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Comment: C: How to create B-allele frequency file for ADTEx?
6.9 years ago by Dataman ▴ 350
6
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5
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4.1k
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How to create B-allele frequency file for ADTEx?
next-gen sequencing exome adtex
updated 6.9 years ago by 5.6k • written 6.9 years ago by ▴ 350
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2.7k
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Comment: C: exome cnv analysis of cases only
7.2 years ago by Dataman ▴ 350
11
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1
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4.0k
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Does one need to sort and index after performing a rmdup in Samtools?
sequencing alignment samtools variant
updated 4 weeks ago by 36k • written 7.3 years ago by ▴ 350
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2.6k
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Answer: Answer: Estimating the expected number of reads that overlap a [heterozygous] snp in one
updated 4 months ago by 36k • written 7.6 years ago by ▴ 350
2
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1
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2.6k
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Estimating the expected number of reads that overlap a [heterozygous] snp in one window from the read depth, read length and resolution
statistics allele simualtion snp baf
updated 4 months ago by 36k • written 7.7 years ago by ▴ 350
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4.5k
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Comment: Comment: Simulating Read Depth
updated 5 months ago by 36k • written 7.8 years ago by ▴ 350
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1
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2.2k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 6 months ago by 36k • written 7.8 years ago by ▴ 350
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1
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2.2k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 6 months ago by 36k • written 7.8 years ago by ▴ 350
6
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7
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2.2k
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Why is the noise level higher in regions with amplification than regions with deletion in the genome?
dna-seq allele fraction tool snp noise
updated 6 months ago by 36k • written 7.8 years ago by ▴ 350
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2.2k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 6 months ago by 36k • written 7.8 years ago by ▴ 350
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