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5.4k
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Comment: C: STAR-2 PASS raw read mapping for SNP calling using GATK
8.6 years ago by WouterDeCoster 48k
0
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0
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3.1k
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Comment: C: select DE genes
8.6 years ago by WouterDeCoster 48k
3
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1
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3.0k
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Answer: C: When I am trying to copy 9GB BAM files to the hard disk, the copied BAM file has
8.6 years ago by WouterDeCoster 48k
0
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0
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3.0k
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Comment: C: When I am trying to copy 9GB BAM files to the hard disk, the copied BAM file has
8.6 years ago by WouterDeCoster 48k
0
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2
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3.1k
views
Comment: C: select DE genes
8.6 years ago by WouterDeCoster 48k
2
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1
reply
3.1k
views
Comment: C: select DE genes
8.6 years ago by WouterDeCoster 48k
0
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1
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3.5k
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Answer: A: samtools updation in linux
8.6 years ago by WouterDeCoster 48k
0
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0
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1.1k
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Comment: C: Initial user of circos
8.6 years ago by WouterDeCoster 48k
1
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0
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1.5k
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Comment: C: Looking for BAM files of the mm10 genome
8.6 years ago by WouterDeCoster 48k
0
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1
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3.4k
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Comment: C: Tophat 2.1.1 failing to recognize fasta file
8.6 years ago by WouterDeCoster 48k
0
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0
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2.6k
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Comment: C: how to correct chromosome number and variant position in a VCF file by the rs#?
8.6 years ago by WouterDeCoster 48k
0
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0
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1.8k
views
Comment: C: Query related to GATK
8.6 years ago by WouterDeCoster 48k
2
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1
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4.9k
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Comment: C: Calculating fold change
8.6 years ago by WouterDeCoster 48k
0
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0
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3.1k
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Comment: C: How to get the number of exon within genes from GRCH37 reference
8.6 years ago by WouterDeCoster 48k
0
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1
reply
1.8k
views
Comment: C: sequences data QC
8.6 years ago by WouterDeCoster 48k
3
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0
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2.0k
views
Comment: C: Getting No. of reads from BAM by pysam (ChIP-seq)
8.6 years ago by WouterDeCoster 48k
0
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0
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1.2k
views
Comment: C: Quick check of the RNASeq length for a bunch of files
8.6 years ago by WouterDeCoster 48k
0
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0
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4.5k
views
Comment: C: Somatic variant call
8.6 years ago by WouterDeCoster 48k
0
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1
reply
1.7k
views
Comment: C: Exact docking process for mrna cleavage by micrornas
8.6 years ago by WouterDeCoster 48k
1
vote
1
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1.4k
views
Comment: C: The maximum number of CG within 300bp in human genome
8.6 years ago by WouterDeCoster 48k
0
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0
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2.8k
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Comment: C: Variant callers reporting different read depth on same alignment
8.6 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: Someone has experience with KNIFE software for circRNA detection?
8.6 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: R multiple parameters
8.6 years ago by WouterDeCoster 48k
3
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2
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3.2k
views
Answer: C: Someone has experience with KNIFE software for circRNA detection?
8.6 years ago by WouterDeCoster 48k
0
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1
reply
3.2k
views
Comment: C: Web apollo installation not working
8.6 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: Web apollo installation not working
8.6 years ago by WouterDeCoster 48k
0
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0
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2.5k
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Comment: C: Two color microarray Heatmap
8.6 years ago by WouterDeCoster 48k
0
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0
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1.8k
views
Answer: A: Synonymous variants annotated using Variant studio not having HGVS p. amino acid
8.6 years ago by WouterDeCoster 48k
0
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1
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6.0k
views
Comment: C: Allele frequency of a gene from a .bam file.
8.6 years ago by WouterDeCoster 48k
1
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0
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2.3k
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Comment: C: SNP for RNA-Seq
8.6 years ago by WouterDeCoster 48k
0
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0
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2.0k
views
Comment: C: how to incorporate the gene ids/in tophat query
8.6 years ago by WouterDeCoster 48k
1
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0
replies
6.0k
views
Comment: C: Shortening fasta sequence names
8.6 years ago by WouterDeCoster 48k
0
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1
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2.9k
views
Answer: A: How to align non overlapping fastq files
8.6 years ago by WouterDeCoster 48k
0
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1
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2.2k
views
Comment: C: cuff merge does not run
8.6 years ago by WouterDeCoster 48k
1
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0
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6.0k
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Comment: C: shartening fasta sequence names
8.6 years ago by WouterDeCoster 48k
0
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0
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2.4k
views
Comment: C: Filter sam file to remove reads with large deletions
8.6 years ago by WouterDeCoster 48k
3
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1
reply
15k
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Comment: C: Getting edit distance from sam tags MD & NM: conceptual misunderstanding?
8.6 years ago by WouterDeCoster 48k
0
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1
reply
5.1k
views
Comment: C: How to analyze CAGE-Seq data?
8.6 years ago by WouterDeCoster 48k
0
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1
reply
3.3k
views
Comment: C: Read a text file into a list
8.6 years ago by WouterDeCoster 48k
1
vote
1
reply
2.8k
views
Comment: C: Heatmap for DEG data
8.6 years ago by WouterDeCoster 48k
1
vote
0
replies
2.7k
views
Comment: C: Agilent focused exome panel supplementary data ?
8.6 years ago by WouterDeCoster 48k
0
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0
replies
1.7k
views
Comment: C: HTseq report 80% of reads no feature
8.6 years ago by WouterDeCoster 48k
0
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0
replies
2.7k
views
Comment: C: Which tool for detection of VNTR?
8.6 years ago by WouterDeCoster 48k
0
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1
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2.7k
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Comment: C: Which tool for detection of VNTR?
8.6 years ago by WouterDeCoster 48k
0
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1
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3.7k
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Comment: C: CNV / SV Filtration
8.6 years ago by WouterDeCoster 48k
0
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0
replies
2.0k
views
Comment: C: Arranging header in nr database via Python (Unable to input multiple files)
8.6 years ago by WouterDeCoster 48k
0
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1
reply
3.7k
views
Comment: C: CNV / SV Filtration
8.6 years ago by WouterDeCoster 48k
1
vote
0
replies
2.0k
views
Comment: C: how to incorporate the gene ids/in tophat query
8.6 years ago by WouterDeCoster 48k
3
votes
0
replies
2.0k
views
Answer: C: Arranging header in nr database via Python (Unable to input multiple files)
8.6 years ago by WouterDeCoster 48k
0
votes
1
reply
2.8k
views
Comment: C: Heatmap for DEG data
8.6 years ago by WouterDeCoster 48k
7,263 results • Page 86 of 146
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