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27k
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Comment: C: Extracting List Of Genes Associated With A Pathway In Kegg
8.9 years ago by Dataman ▴ 380
0
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0
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1.7k
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Comment: C: rename Fasta file headings for use in MIRA
8.9 years ago by Dataman ▴ 380
2
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1
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6.7k
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Comment: C: Beginner in Bioinformatics / computational biology field
8.9 years ago by Dataman ▴ 380
0
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1
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7.3k
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Answer: Answer: txt file to bigwig
9 months ago by Dataman ▴ 380
1
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0
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29k
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Comment: C: samtools bedcov vs. bedtools coverage
8.9 years ago by Dataman ▴ 380
0
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0
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29k
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Comment: C: samtools bedcov vs. bedtools coverage
8.9 years ago by Dataman ▴ 380
0
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0
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29k
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Comment: C: samtools bedcov vs. bedtools coverage
9.0 years ago by Dataman ▴ 380
0
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0
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29k
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Comment: C: samtools bedcov vs. bedtools coverage
9.0 years ago by Dataman ▴ 380
1
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0
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11k
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Answer: A: Gene set enrichment tool for RNA-Seq in Python?
9.0 years ago by Dataman ▴ 380
0
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1
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4.4k
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Comment: C: what does Num_Probes in a segmentation file refer to?
9.2 years ago by Dataman ▴ 380
1
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1
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4.4k
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Comment: C: what does Num_Probes in a segmentation file refer to?
9.2 years ago by Dataman ▴ 380
5
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5
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4.4k
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what does Num_Probes in a segmentation file refer to?
sequencing
updated 9.2 years ago by ★ 3.0k • written 9.2 years ago by ▴ 380
0
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0
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7.3k
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Comment: C: CNA calculation from Segmentation file
9.2 years ago by Dataman ▴ 380
0
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0
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17k
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Comment: C: TCGA Segement Mean, GISTIC and CNVs
9.2 years ago by Dataman ▴ 380
19
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15
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9.2k
views
6 follow
What is the best way to make a bam file smaller by removing unwanted information?
bam next-gen-sequencing
updated 2.8 years ago by 45k • written 9.3 years ago by ▴ 380
0
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0
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9.2k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
9.3 years ago by Dataman ▴ 380
0
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1
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9.2k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
9.3 years ago by Dataman ▴ 380
1
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1
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9.2k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
9.3 years ago by Dataman ▴ 380
0
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0
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13k
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Comment: Comment: Is There Any Reference Exome ?
updated 2.4 years ago by 45k • written 9.9 years ago by ▴ 380
0
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0
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5.5k
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Comment: C: How to create B-allele frequency file for ADTEx?
9.9 years ago by Dataman ▴ 380
6
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5
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5.5k
views
How to create B-allele frequency file for ADTEx?
adtex next-gen-sequencing
updated 2.4 years ago by 45k • written 9.9 years ago by ▴ 380
0
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0
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3.9k
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Comment: Comment: exome cnv analysis of cases only
updated 3.0 years ago by 45k • written 10.2 years ago by ▴ 380
11
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1
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5.2k
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Does one need to sort and index after performing a rmdup in Samtools?
sequencing alignment samtools variant
updated 3.1 years ago by 45k • written 10.3 years ago by ▴ 380
1
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0
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3.2k
views
Answer: Answer: Estimating the expected number of reads that overlap a [heterozygous] snp in one
updated 3.4 years ago by 45k • written 10.6 years ago by ▴ 380
2
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1
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3.2k
views
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 3.4 years ago by 45k • written 10.7 years ago by ▴ 380
0
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0
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6.1k
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Comment: Comment: Simulating Read Depth
updated 3.4 years ago by 45k • written 10.8 years ago by ▴ 380
0
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1
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3.2k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 3.5 years ago by 45k • written 10.8 years ago by ▴ 380
0
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1
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3.2k
views
Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 3.5 years ago by 45k • written 10.8 years ago by ▴ 380
6
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7
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3.2k
views
Why is the noise level higher in regions with amplification than regions with deletion in the genome?
snp dna-seq allele-fraction
updated 23 months ago by 45k • written 10.8 years ago by ▴ 380
0
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0
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3.2k
views
Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 3.5 years ago by 45k • written 10.8 years ago by ▴ 380
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