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Comment: C: reliable way to trim
6.5 years ago by WouterDeCoster 48k
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2.8k
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Comment: C: reliable way to trim
6.5 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Comment: C: reliable way to trim
6.5 years ago by WouterDeCoster 48k
0
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2
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3.0k
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Comment: C: Can I ignore these MSTRG genes in downstream analysis (pantherdb.org)?
6.5 years ago by WouterDeCoster 48k
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1.4k
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Comment: C: Problem with installation of msms
6.5 years ago by WouterDeCoster 48k
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1
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1.4k
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Comment: C: Problem with installation of msms
6.5 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Comment: C: reliable way to trim
6.5 years ago by WouterDeCoster 48k
0
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1
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1.1k
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Comment: C: Coverage calulation for each transcripts for variant analysis in RNA-seq data
6.5 years ago by WouterDeCoster 48k
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1
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2.0k
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Comment: C: How to predict non-sense mediated decay from Illumina reads?
6.5 years ago by WouterDeCoster 48k
1
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2.0k
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Comment: C: How to predict non-sense mediated decay from Illumina reads?
6.5 years ago by WouterDeCoster 48k
0
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1
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2.0k
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Comment: C: How to predict non-sense mediated decay from Illumina reads?
6.5 years ago by WouterDeCoster 48k
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2
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5.3k
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Comment: C: RNA-seq: is there a way to get the variability between biological replicates ?
6.5 years ago by WouterDeCoster 48k
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2.0k
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Comment: C: Extract fasta files that are not empty from a directory and subdirectories
6.5 years ago by WouterDeCoster 48k
2
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2
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5.3k
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Answer: C: RNA-seq: is there a way to get the variability between biological replicates ?
6.5 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: C: Tassel Hapmap Format Query
6.5 years ago by WouterDeCoster 48k
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0
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1.6k
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Comment: C: Link mice RNA-seq data to proteins
6.5 years ago by WouterDeCoster 48k
1
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1
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1.6k
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Comment: C: Link mice RNA-seq data to proteins
6.5 years ago by WouterDeCoster 48k
1
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2.2k
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Answer: A: Replace @RG group by the one of another BAM
6.5 years ago by WouterDeCoster 48k
0
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1
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2.9k
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Comment: C: Following the GATK recommended workflow for DNA sequence data, my mpileup output
6.5 years ago by WouterDeCoster 48k
0
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0
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999
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Answer: A: high frequency protein truncating variants in hg19
6.5 years ago by WouterDeCoster 48k
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0
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2.5k
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Comment: C: DE analysis with edgeR and possibly batch effect
6.5 years ago by WouterDeCoster 48k
0
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0
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13k
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Comment: C: Hardware requirement for RNA-seq
6.5 years ago by WouterDeCoster 48k
1
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0
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1.8k
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Comment: C: Cufflinks transcriptome (To build or not to build?)
6.5 years ago by WouterDeCoster 48k
1
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0
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793
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Comment: C: aa index finding
6.5 years ago by WouterDeCoster 48k
0
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1
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1.3k
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Comment: C: Grad school help: Transcriptomics and Pathways Analysis
6.5 years ago by WouterDeCoster 48k
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3.1k
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Answer: A: DEG from BAM file
6.5 years ago by WouterDeCoster 48k
0
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1
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2.6k
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Comment: C: Htseq-count result assistance
6.5 years ago by WouterDeCoster 48k
2
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6.2k
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Comment: C: What does CSQ means in a VCF file annotated by VEP ?
6.5 years ago by WouterDeCoster 48k
6
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1
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6.2k
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Answer: A: What does CSQ means in a VCF file annotated by VEP ?
6.5 years ago by WouterDeCoster 48k
0
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0
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2.6k
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Comment: C: Htseq-count result assistance
6.5 years ago by WouterDeCoster 48k
1
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0
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2.6k
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Comment: C: Htseq-count result assistance
6.5 years ago by WouterDeCoster 48k
0
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0
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2.4k
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Comment: C: Extract coverage from each nucleotide position of a genome in a bam file
6.5 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: I am not able to install CNVkit
6.5 years ago by WouterDeCoster 48k
0
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0
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884
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Comment: C: indexerror of afterqc for quality control
6.5 years ago by WouterDeCoster 48k
1
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0
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1.3k
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Comment: C: Two-way cross family analysis for ranked combinations
6.5 years ago by WouterDeCoster 48k
1
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0
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1.5k
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Comment: C: Filtering fpkm values for two group separetly
6.5 years ago by WouterDeCoster 48k
0
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1
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1.4k
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Comment: C: sam2rma error while doing metagenomics analysis
6.5 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: C: I need some tips and suggestions for further analysis of NGS expression data (lo
6.5 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: C: I need some tips and suggestions for further analysis of NGS expression data (lo
6.5 years ago by WouterDeCoster 48k
0
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0
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6.1k
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Comment: C: rowVars function, used in ballgown analysis not available for R 3.5.2, alternati
6.5 years ago by WouterDeCoster 48k
0
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0
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7.5k
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Comment: C: Ideal data amounts and read depth generated by MinION sequencer
6.5 years ago by WouterDeCoster 48k
1
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1
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2.1k
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Comment: C: extract difference gene from two platform
6.6 years ago by WouterDeCoster 48k
0
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0
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1.9k
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Comment: C: PARSE by gene name in biopython
6.6 years ago by WouterDeCoster 48k
0
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0
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1.9k
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Comment: C: PARSE by gene name in biopython
6.6 years ago by WouterDeCoster 48k
0
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0
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1.8k
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Comment: C: Need sample vcf file containing Complete Exome sequences
6.6 years ago by WouterDeCoster 48k
5
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1
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1.9k
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Answer: A: Writing a batch script for analyzing RNA-Seq data
6.6 years ago by WouterDeCoster 48k
0
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0
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9.2k
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Comment: C: fq.gz file use
6.6 years ago by WouterDeCoster 48k
1
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1
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2.1k
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Comment: C: extract difference gene from two platform
6.6 years ago by WouterDeCoster 48k
1
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0
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2.1k
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Comment: C: multiple FASTA sequnces in to one full sequnce according to their chromosome num
6.6 years ago by WouterDeCoster 48k
0
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1
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2.4k
views
Comment: C: picard not working whatever I am trying
6.6 years ago by WouterDeCoster 48k
7,263 results • Page 20 of 146
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