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Comment: Comment: Low quality fast5 files
2.6 years ago by WouterDeCoster 47k
1
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1
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1.1k
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Comment: Comment: Michigan Imputation Server does not impute all input files
2.6 years ago by WouterDeCoster 47k
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1
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1.8k
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Comment: Comment: Beagle 5 error: No VCF records found in the specified interval
2.6 years ago by WouterDeCoster 47k
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1
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945
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Comment: Comment: About Foreign Fields in VCF (4.3)
2.6 years ago by WouterDeCoster 47k
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1
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5.6k
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Comment: Comment: How to write a Python script to edit a .vcf file?
2.6 years ago by WouterDeCoster 47k
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1
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1.6k
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Comment: Comment: What current tools are used to phase haplotypes from a FASTQ file?
2.6 years ago by WouterDeCoster 47k
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1.6k
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Comment: Comment: What current tools are used to phase haplotypes from a FASTQ file?
2.6 years ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: How are two alleles typically represented in a whole genome sequence?
2.6 years ago by WouterDeCoster 47k
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241k
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Answer: Answer: Tools To Calculate Average Coverage For A Bam File?
2.7 years ago by WouterDeCoster 47k
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1
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736
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Comment: Comment: Help me do a gene enrichment analysis
2.7 years ago by WouterDeCoster 47k
1
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1
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893
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Comment: Comment: hisat2 | samtools server vs cluster error
2.7 years ago by WouterDeCoster 47k
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1
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658
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Comment: Comment: Gene Expression Threshold
2.7 years ago by WouterDeCoster 47k
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1.3k
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Answer: Answer: Validation of somatic variant calling pipeline
2.8 years ago by WouterDeCoster 47k
2
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0
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990
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Comment: Comment: Samtools difference between Mapped and Unmapped read
2.8 years ago by WouterDeCoster 47k
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3.6k
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Comment: Comment: How do I detect deletions?
2.8 years ago by WouterDeCoster 47k
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1
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748
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Answer: Answer: inquiry related to rsid
2.8 years ago by WouterDeCoster 47k
1
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1
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1.3k
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Comment: Comment: What does "viewpoint" mean?
2.9 years ago by WouterDeCoster 47k
0
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0
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874
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Comment: Comment: Why are there nucleotides in the reference genome which are also minor alleles i
2.9 years ago by WouterDeCoster 47k
0
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1
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1.2k
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Comment: Comment: Finding the sex of of an individual from an NGS output
2.9 years ago by WouterDeCoster 47k
2
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2
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874
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Answer: Answer: Why are there nucleotides in the reference genome which are also minor alleles i
2.9 years ago by WouterDeCoster 47k
1
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1
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1.2k
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Answer: Answer: Finding the sex of of an individual from an NGS output
2.9 years ago by WouterDeCoster 47k
1
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0
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1.4k
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Comment: Comment: Converting .delta file from NUCMER to format accepted by IGV? (.bam/.vcf)
2.9 years ago by WouterDeCoster 47k
1
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0
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1.1k
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Comment: Comment: Bioinformatics Definitions
2.9 years ago by WouterDeCoster 47k
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1
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2.0k
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Comment: Comment: how to align fastq files to a fasta file using biopython to produce VCF file
2.9 years ago by WouterDeCoster 47k
0
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1
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759
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Comment: Comment: Corset error
2.9 years ago by WouterDeCoster 47k
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0
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827
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Comment: Comment: extract the ids and key values
2.9 years ago by WouterDeCoster 47k
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0
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1.7k
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Comment: Comment: How to search for genes 100Kb up and downstream of any genomic site
2.9 years ago by WouterDeCoster 47k
1
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0
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627
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Comment: Comment: What tools are best for conjoined gene/readthough detection and how do they diff
2.9 years ago by WouterDeCoster 47k
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1
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1.1k
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Comment: Comment: FeatureCounts Number of Reads
2.9 years ago by WouterDeCoster 47k
1
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0
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15k
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Comment: Comment: How to trim Nanopore reads. Please suggest a tool.
3.0 years ago by WouterDeCoster 47k
3
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1
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2.3k
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Answer: Answer: How to create a subset from a Nanopore fast5 file?
3.0 years ago by WouterDeCoster 47k
0
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0
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700
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Job: PhD position: bioinformatics analysis of omics data in frontotemporal dementia
genetics phd
updated 11 months ago by 44k • written 3.0 years ago by 47k
1
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1
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834
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Comment: Comment: whole tissue and RNA-seq: can I still study specific cell types?
3.0 years ago by WouterDeCoster 47k
1
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1
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834
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Comment: Comment: whole tissue and RNA-seq: can I still study specific cell types?
3.0 years ago by WouterDeCoster 47k
0
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1
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1.7k
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Comment: Comment: Hello everyone whenever i run this command this error terminates the command. ca
3.0 years ago by WouterDeCoster 47k
1
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2
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1.7k
views
Comment: Comment: Hello everyone whenever i run this command this error terminates the command. ca
3.0 years ago by WouterDeCoster 47k
1
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1
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3.5k
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Comment: Comment: How to install argparse for python 2.7
3.0 years ago by WouterDeCoster 47k
0
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0
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10k
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Comment: Comment: Change header of a Fasta file according to the file name
3.0 years ago by WouterDeCoster 47k
0
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1
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2.5k
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Comment: Comment: How to interpret a FASTA file
3.0 years ago by WouterDeCoster 47k
0
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0
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2.5k
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Comment: Comment: How to interpret a FASTA file
updated 3.0 years ago by 15k • written 3.0 years ago by 47k
2
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1
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3.2k
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Comment: Comment: Trimming on Nanopore Data
3.0 years ago by WouterDeCoster 47k
0
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0
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753
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Comment: Comment: How to use python to align 30 kb genome to another 30kb reference, repeat 10x ti
3.0 years ago by WouterDeCoster 47k
1
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0
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1.5k
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Comment: Comment: whatsHap didn't phase all variants
3.0 years ago by WouterDeCoster 47k
0
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0
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2.6k
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Comment: Comment: What are the columns from pysam fetch?
3.0 years ago by WouterDeCoster 47k
1
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0
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1.3k
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Comment: Comment: VCF filtering
3.0 years ago by WouterDeCoster 47k
0
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1
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1.4k
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Answer: Answer: How to do a pairwise alignment and convert the result to a VCF file?
3.0 years ago by WouterDeCoster 47k
0
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0
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1.7k
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Comment: Comment: reference fasta creation
3.0 years ago by WouterDeCoster 47k
2
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0
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405
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Comment: Comment: Compatilibity between human37 and human38 gtf
3.1 years ago by WouterDeCoster 47k
1
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0
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1.4k
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Comment: Comment: Variable numbers of Reads. I'm lost
3.1 years ago by WouterDeCoster 47k
0
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0
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814
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Comment: Comment: Does GISAID fasta files contain spike protein or whole genome sequence?
3.1 years ago by WouterDeCoster 47k
7,255 results • Page 3 of 146
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