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Comment: C: Extracting List Of Genes Associated With A Pathway In Kegg
7.2 years ago by Dataman ▴ 370
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1.3k
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Comment: C: rename Fasta file headings for use in MIRA
7.3 years ago by Dataman ▴ 370
2
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1
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5.7k
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Comment: C: Beginner in Bioinformatics / computational biology field
7.3 years ago by Dataman ▴ 370
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4.6k
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Answer: A: txt file to bigwig
7.3 years ago by Dataman ▴ 370
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4.6k
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Comment: C: txt file to bigwig
7.3 years ago by Dataman ▴ 370
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25k
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Comment: C: samtools bedcov vs. bedtools coverage
7.3 years ago by Dataman ▴ 370
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25k
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Comment: C: samtools bedcov vs. bedtools coverage
7.3 years ago by Dataman ▴ 370
0
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0
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25k
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Comment: C: samtools bedcov vs. bedtools coverage
7.3 years ago by Dataman ▴ 370
0
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0
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25k
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Comment: C: samtools bedcov vs. bedtools coverage
7.3 years ago by Dataman ▴ 370
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12k
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Comment: C: Get Snp Position From A Python Interface.
7.4 years ago by Dataman ▴ 370
1
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9.6k
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Answer: A: Gene set enrichment tool for RNA-Seq in Python?
7.4 years ago by Dataman ▴ 370
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1
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3.7k
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Comment: C: what does Num_Probes in a segmentation file refer to?
7.5 years ago by Dataman ▴ 370
1
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1
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3.7k
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Comment: C: what does Num_Probes in a segmentation file refer to?
7.5 years ago by Dataman ▴ 370
5
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5
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3.7k
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what does Num_Probes in a segmentation file refer to?
sequencing
updated 7.5 years ago by ★ 3.0k • written 7.5 years ago by ▴ 370
0
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5.8k
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Comment: C: CNA calculation from Segmentation file
7.5 years ago by Dataman ▴ 370
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0
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16k
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Comment: C: TCGA Segement Mean, GISTIC and CNVs
7.5 years ago by Dataman ▴ 370
19
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15
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6.5k
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6 follow
What is the best way to make a bam file smaller by removing unwanted information?
bam next-gen-sequencing
updated 14 months ago by 40k • written 7.7 years ago by ▴ 370
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6.5k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
7.7 years ago by Dataman ▴ 370
0
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1
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6.5k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
7.7 years ago by Dataman ▴ 370
1
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1
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6.5k
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Comment: C: What is the best way to make a bam file smaller by removing unwanted information
7.7 years ago by Dataman ▴ 370
0
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11k
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Comment: Comment: Is There Any Reference Exome ?
updated 9 months ago by 40k • written 8.3 years ago by ▴ 370
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4.7k
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Comment: C: How to create B-allele frequency file for ADTEx?
8.3 years ago by Dataman ▴ 370
6
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5
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4.7k
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How to create B-allele frequency file for ADTEx?
adtex next-gen-sequencing
updated 9 months ago by 40k • written 8.3 years ago by ▴ 370
0
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3.2k
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Comment: Comment: exome cnv analysis of cases only
updated 16 months ago by 40k • written 8.5 years ago by ▴ 370
11
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1
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4.6k
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Does one need to sort and index after performing a rmdup in Samtools?
sequencing alignment samtools variant
updated 17 months ago by 40k • written 8.6 years ago by ▴ 370
1
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2.9k
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Answer: Answer: Estimating the expected number of reads that overlap a [heterozygous] snp in one
updated 21 months ago by 40k • written 9.0 years ago by ▴ 370
2
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1
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2.9k
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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 21 months ago by 40k • written 9.1 years ago by ▴ 370
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5.0k
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Comment: Comment: Simulating Read Depth
updated 21 months ago by 40k • written 9.1 years ago by ▴ 370
0
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1
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2.6k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 22 months ago by 40k • written 9.2 years ago by ▴ 370
0
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1
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2.6k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 22 months ago by 40k • written 9.2 years ago by ▴ 370
6
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7
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2.6k
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Why is the noise level higher in regions with amplification than regions with deletion in the genome?
snp dna-seq allele-fraction
updated 3 months ago by 40k • written 9.2 years ago by ▴ 370
0
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0
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2.6k
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Comment: Comment: Why is the noise level higher in regions with amplification than regions with d
updated 22 months ago by 40k • written 9.2 years ago by ▴ 370
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