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Comment: C: How to compare two very different NGS samples?
8.4 years ago by WouterDeCoster 48k
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2.5k
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Comment: C: T Cell Repertoire Deep Sequencing
8.4 years ago by WouterDeCoster 48k
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12k
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Comment: C: Stranger Things: unexpected limitations of popular tools
8.4 years ago by WouterDeCoster 48k
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1.8k
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Comment: C: counting the reads mapped only to the coding sequence
8.4 years ago by WouterDeCoster 48k
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1
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6.1k
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Comment: C: Marker genes for different cell types
8.4 years ago by WouterDeCoster 48k
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1
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14k
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Comment: C: Is there any way to install RStudio (or any other powerful IDE for R) without ro
8.4 years ago by WouterDeCoster 48k
2
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5.4k
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Comment: C: Amplicon Sequencing Data Analysis
8.4 years ago by WouterDeCoster 48k
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2.9k
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Comment: C: REsequencing Genome Assembly and Functional Gene annotation workflow?
8.4 years ago by WouterDeCoster 48k
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1.6k
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Answer: A: variable regions within exons of a gene
8.4 years ago by WouterDeCoster 48k
1
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1
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2.9k
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Comment: C: REsequencing Genome Assembly and Functional Gene annotation workflow?
8.4 years ago by WouterDeCoster 48k
2
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0
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14k
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Comment: C: Is there any way to install RStudio (or any other powerful IDE for R) without ro
8.4 years ago by WouterDeCoster 48k
5
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2
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14k
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Answer: A: Is there any way to install RStudio (or any other powerful IDE for R) without ro
8.4 years ago by WouterDeCoster 48k
1
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0
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1.9k
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Answer: A: Flag job posts when position has been filled
8.4 years ago by WouterDeCoster 48k
0
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1
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14k
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Comment: C: Is there any way to install RStudio (or any other powerful IDE for R) without ro
8.4 years ago by WouterDeCoster 48k
0
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0
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4.1k
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Comment: C: samtools sort stuck during merging
8.4 years ago by WouterDeCoster 48k
2
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1
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4.1k
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Comment: C: samtools sort stuck during merging
8.4 years ago by WouterDeCoster 48k
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1
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2.7k
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Comment: C: CAGEr BAM files size issue
8.4 years ago by WouterDeCoster 48k
2
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1
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1.8k
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Comment: C: Confusing allele notation for SNP data
8.4 years ago by WouterDeCoster 48k
0
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3.6k
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Comment: C: bam-readcount empty output
8.4 years ago by WouterDeCoster 48k
2
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0
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2.7k
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Comment: C: About the reads aligned 0 times (around 10%) in Bowtie2.
8.4 years ago by WouterDeCoster 48k
0
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1
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2.7k
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Comment: C: CAGEr BAM files size issue
8.4 years ago by WouterDeCoster 48k
5
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2
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5.4k
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Answer: A: Amplicon Sequencing Data Analysis
8.4 years ago by WouterDeCoster 48k
0
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0
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2.0k
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Comment: C: spliced alignment algorithm
8.4 years ago by WouterDeCoster 48k
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0
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2.0k
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Comment: C: SNP array liftover data with p values
8.4 years ago by WouterDeCoster 48k
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3.0k
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Comment: C: What is new in samtools release 1.5 [Solstice Release] (21st June 2017)
8.4 years ago by WouterDeCoster 48k
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0
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2.0k
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Comment: C: Problem in extraction of values from a list
8.4 years ago by WouterDeCoster 48k
3
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1
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2.0k
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Answer: C: Problem in extraction of values from a list
8.4 years ago by WouterDeCoster 48k
0
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1
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2.0k
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Answer: A: Problem in extraction of values from a list
8.4 years ago by WouterDeCoster 48k
0
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0
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2.0k
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Comment: C: Problem in extraction of values from a list
8.4 years ago by WouterDeCoster 48k
0
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1
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2.0k
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Comment: C: sorting out the common path in a python script with different functions
8.4 years ago by WouterDeCoster 48k
1
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0
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2.0k
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Comment: C: sorting out the common path in a python script with different functions
8.4 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: Human in NCBI Genomes
8.4 years ago by WouterDeCoster 48k
0
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1
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3.6k
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Comment: C: Illumina sequencing - paired end reads
8.4 years ago by WouterDeCoster 48k
2
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1
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4.0k
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Comment: C: Use kallisto with ONT (nanopore) cDNA long reads
8.4 years ago by WouterDeCoster 48k
0
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1
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4.0k
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Comment: C: Use kallisto with ONT (nanopore) cDNA long reads
8.4 years ago by WouterDeCoster 48k
0
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1
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1.8k
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Comment: C: Should PARs be hard-masked in human genome while using htseq-count for downstre
8.4 years ago by WouterDeCoster 48k
1
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0
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2.1k
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Comment: C: How to check if specific mutations are or not enriched in a RNAseq data seq?
8.4 years ago by WouterDeCoster 48k
2
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0
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2.0k
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Answer: A: which annotation to use and is it advisable to use bam to fastq
8.4 years ago by WouterDeCoster 48k
0
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1
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1.5k
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Comment: C: Finding common small RNAs between two FASTQ datasets.
8.4 years ago by WouterDeCoster 48k
0
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1
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6.7k
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Comment: C: Assembling PacBio reads using a reference genome
8.4 years ago by WouterDeCoster 48k
0
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1
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3.4k
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Comment: C: GMAP v2017-06-20 error
8.4 years ago by WouterDeCoster 48k
3
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0
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3.0k
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Comment: C: CNVkit GRCh38 tumor-normal pair
8.4 years ago by WouterDeCoster 48k
0
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0
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24k
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Comment: C: TCGA UUIDS to TCGA barcode (SampleID) in R
8.4 years ago by WouterDeCoster 48k
0
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1
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6.3k
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Comment: C: Yet Another Programming Language
8.4 years ago by WouterDeCoster 48k
4
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1
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2.3k
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Answer: A: how can I keep only those SNP in file "a" which match to SNPs in file "b"?
8.4 years ago by WouterDeCoster 48k
0
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1
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7.8k
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Comment: C: Remove the last few bases from fasta sequences
8.4 years ago by WouterDeCoster 48k
0
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0
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7.8k
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Comment: C: Remove the last few bases from fasta sequences
8.4 years ago by WouterDeCoster 48k
1
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0
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7.8k
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Comment: C: Remove the last few bases from fasta sequences
8.4 years ago by WouterDeCoster 48k
0
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1
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1.6k
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Comment: C: Query about bioinformatics service
8.4 years ago by WouterDeCoster 48k
0
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1
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2.4k
views
Comment: C: Cuffdiff fatal error exit code- 134 ()
8.4 years ago by WouterDeCoster 48k
7,263 results • Page 73 of 146
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