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3.0k
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Comment: C: DEXSeq Installation Error
5.9 years ago by WouterDeCoster 48k
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0
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1.3k
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Comment: C: Reconstruct reference sequence from SAM file?
5.9 years ago by WouterDeCoster 48k
1
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2
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1.3k
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Answer: A: Reconstruct reference sequence from SAM file?
5.9 years ago by WouterDeCoster 48k
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1
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2.6k
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Answer: A: Aligning multiple Fastq files using Bowtie2
5.9 years ago by WouterDeCoster 48k
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0
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2.2k
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Comment: C: soft-clipping during alignment and variant calling query
5.9 years ago by WouterDeCoster 48k
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0
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2.7k
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Comment: C: TCGA data analysis: DEG analysis
5.9 years ago by WouterDeCoster 48k
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1.4k
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Job: Three PI positions in neurogenomics or neuroscience at VIB-UAntwerp (Belgium)
VIB neuroscience genomics
updated 2.3 years ago by 45k • written 6.0 years ago by 48k
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1
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7.3k
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Comment: C: pysam alignment error
5.9 years ago by WouterDeCoster 48k
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0
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1.3k
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Comment: C: How does base quality / mapping quality affect germline calling
5.9 years ago by WouterDeCoster 48k
1
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0
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1.3k
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Comment: C: DEG without replicates
5.9 years ago by WouterDeCoster 48k
0
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0
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985
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Comment: C: How to calculate the p-value of frequency of my study and control of some varian
5.9 years ago by WouterDeCoster 48k
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0
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4.4k
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Comment: C: Retrieve multi-line fasta sequences using list of locus tag
updated 5.9 years ago by 16k • written 7.3 years ago by 48k
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0
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1.7k
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Comment: C: List of genes with common false-positives
6.0 years ago by WouterDeCoster 48k
0
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1
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1.7k
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Comment: C: List of genes with common false-positives
6.0 years ago by WouterDeCoster 48k
0
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1
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2.8k
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Comment: C: How to create a dna database that can be analyze with R ?
6.0 years ago by WouterDeCoster 48k
0
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0
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1.9k
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Comment: C: hap.py roc curve plot
6.0 years ago by WouterDeCoster 48k
0
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1
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1.8k
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Comment: C: Call fusion genes from WES data
6.0 years ago by WouterDeCoster 48k
0
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1
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2.7k
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Comment: C: Pipe pysam.view() output to pysam.sort()
6.0 years ago by WouterDeCoster 48k
1
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1
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2.8k
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Comment: C: How to create a dna database that can be analyze with R ?
6.0 years ago by WouterDeCoster 48k
0
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0
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4.1k
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Comment: C: Error when installing bedtools
6.0 years ago by WouterDeCoster 48k
0
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0
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1.0k
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Comment: C: going from the merged bam to original bam files
6.0 years ago by WouterDeCoster 48k
1
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1
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817
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Answer: A: API for searching for adjacent genes
6.0 years ago by WouterDeCoster 48k
1
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1
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1.7k
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Comment: C: Mark duplicate "Picard"
6.0 years ago by WouterDeCoster 48k
1
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1
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6.5k
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Comment: C: Is it possible to retrieve the original reads from a BAM file?
6.0 years ago by WouterDeCoster 48k
1
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0
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2.0k
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Answer: C: Installation error - RNAPLEX
6.0 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Answer: A: [W::bcf_hdr_check_sanity] GL should be declared as Number=G
6.0 years ago by WouterDeCoster 48k
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0
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1.2k
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Comment: C: [Circos] Draw additional circle outside a circle
6.0 years ago by WouterDeCoster 48k
0
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0
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17k
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Comment: C: samtools index error
6.0 years ago by WouterDeCoster 48k
0
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1
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2.3k
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Comment: C: How to control BWA output?
6.0 years ago by WouterDeCoster 48k
2
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0
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1.1k
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Comment: C: Common variants discovery
6.0 years ago by WouterDeCoster 48k
0
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0
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1.2k
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Comment: C: How to get the reads with significant RPM?
6.0 years ago by WouterDeCoster 48k
0
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0
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2.3k
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Comment: C: How to control BWA output?
6.0 years ago by WouterDeCoster 48k
0
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0
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1.2k
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Comment: C: Biscuit: Is alignment stochastic?
6.0 years ago by WouterDeCoster 48k
0
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0
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6.1k
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Comment: C: cram to bam conversion
6.0 years ago by WouterDeCoster 48k
4
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1
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11k
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Comment: C: Python FASTA scripting
6.0 years ago by WouterDeCoster 48k
0
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0
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1.8k
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Comment: C: How to correlate phenotype values with gene expression levels
6.0 years ago by WouterDeCoster 48k
1
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0
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3.4k
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Comment: C: which is good haplotypecaller and UnifiedGenotyper?
updated 6.0 years ago by 5.9k • written 8.1 years ago by 48k
1
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0
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3.3k
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Answer: A: hg19 exon, intron, UTR region
6.0 years ago by WouterDeCoster 48k
0
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0
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1.4k
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Comment: C: New to NGS data Analysis
6.0 years ago by WouterDeCoster 48k
3
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1
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3.7k
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Answer: C: How to properly measure the length of a reference genome
6.0 years ago by WouterDeCoster 48k
0
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1
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3.7k
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Comment: C: How to properly measure the length of a reference genome
6.0 years ago by WouterDeCoster 48k
0
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1
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3.4k
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Comment: C: Getting an empty .fastq file as output when ran poretools command on multiple .f
6.0 years ago by WouterDeCoster 48k
0
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0
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3.4k
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Comment: C: Getting an empty .fastq file as output when ran poretools command on multiple .f
6.0 years ago by WouterDeCoster 48k
0
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1
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3.4k
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Comment: C: Getting an empty .fastq file as output when ran poretools command on multiple .f
6.0 years ago by WouterDeCoster 48k
0
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0
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1.2k
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Comment: C: Is It a Necessity to Remove Human Data from Samples for Metagenomic Analysis?
6.0 years ago by WouterDeCoster 48k
2
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0
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4.3k
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Answer: A: How do I install the R package on GitHub with bioconda
6.0 years ago by WouterDeCoster 48k
1
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0
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3.6k
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Comment: C: Working abroad without a thesis
updated 6.0 years ago by 103k • written 6.0 years ago by 48k
2
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2
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1.2k
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Answer: A: How to get the extended flanking read sequences in the reference based genome as
6.0 years ago by WouterDeCoster 48k
3
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0
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1.4k
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Answer: A: Can I combine RPM values of RNA datasets from tow different databases?
6.0 years ago by WouterDeCoster 48k
0
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1
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3.4k
views
Comment: C: Getting an empty .fastq file as output when ran poretools command on multiple .f
6.0 years ago by WouterDeCoster 48k
7,263 results • Page 11 of 146
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