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Comment: Comment: What are "must have" data types one should extract from WGS .fq data?
3.9 years ago by WouterDeCoster 48k
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Comment: Comment: Biology undergraduate looking for mentor
3.9 years ago by WouterDeCoster 48k
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1.4k
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Comment: Comment: Overlapping bases count in WGS
3.9 years ago by WouterDeCoster 48k
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1.8k
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Comment: Comment: Heterozygous Variants On Male X/Y Chromosome (Exome Data)
3.9 years ago by WouterDeCoster 48k
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Comment: Comment: Heterozygous Variants On Male X/Y Chromosome (Exome Data)
updated 2.6 years ago by 45k • written 3.9 years ago by 48k
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Comment: Comment: Running Hisat2 but it seems not working at all
3.9 years ago by WouterDeCoster 48k
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2.0k
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Comment: Comment: STAR- error
3.9 years ago by WouterDeCoster 48k
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2.0k
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Comment: Comment: A bash question
3.9 years ago by WouterDeCoster 48k
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1.1k
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Comment: Comment: Low quality fast5 files
3.9 years ago by WouterDeCoster 48k
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1.4k
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Comment: Comment: Michigan Imputation Server does not impute all input files
3.9 years ago by WouterDeCoster 48k
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2.5k
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Comment: Comment: Beagle 5 error: No VCF records found in the specified interval
3.9 years ago by WouterDeCoster 48k
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1.3k
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Comment: Comment: About Foreign Fields in VCF (4.3)
3.9 years ago by WouterDeCoster 48k
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8.1k
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Comment: Comment: How to write a Python script to edit a .vcf file?
3.9 years ago by WouterDeCoster 48k
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1
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2.3k
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Comment: Comment: What current tools are used to phase haplotypes from a FASTQ file?
4.0 years ago by WouterDeCoster 48k
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2.3k
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Comment: Comment: What current tools are used to phase haplotypes from a FASTQ file?
4.0 years ago by WouterDeCoster 48k
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1.5k
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Comment: Comment: How are two alleles typically represented in a whole genome sequence?
4.0 years ago by WouterDeCoster 48k
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267k
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Answer: Answer: Tools To Calculate Average Coverage For A Bam File?
4.0 years ago by WouterDeCoster 48k
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1
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1.0k
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Comment: Comment: Help me do a gene enrichment analysis
4.0 years ago by WouterDeCoster 48k
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1.3k
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Comment: Comment: hisat2 | samtools server vs cluster error
4.1 years ago by WouterDeCoster 48k
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886
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Comment: Comment: Gene Expression Threshold
4.1 years ago by WouterDeCoster 48k
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1.9k
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Answer: Answer: Validation of somatic variant calling pipeline
4.1 years ago by WouterDeCoster 48k
2
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1.4k
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Comment: Comment: Samtools difference between Mapped and Unmapped read
4.1 years ago by WouterDeCoster 48k
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6.5k
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Comment: Comment: How do I detect deletions?
4.1 years ago by WouterDeCoster 48k
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1
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1.1k
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Answer: Answer: inquiry related to rsid
4.2 years ago by WouterDeCoster 48k
1
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1.9k
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Comment: Comment: What does "viewpoint" mean?
4.2 years ago by WouterDeCoster 48k
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1.4k
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Comment: Comment: Why are there nucleotides in the reference genome which are also minor alleles i
4.2 years ago by WouterDeCoster 48k
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1
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1.9k
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Comment: Comment: Finding the sex of of an individual from an NGS output
4.2 years ago by WouterDeCoster 48k
2
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2
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1.4k
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Answer: Answer: Why are there nucleotides in the reference genome which are also minor alleles i
4.2 years ago by WouterDeCoster 48k
1
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1
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1.9k
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Answer: Answer: Finding the sex of of an individual from an NGS output
4.2 years ago by WouterDeCoster 48k
1
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0
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1.9k
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Comment: Comment: Converting .delta file from NUCMER to format accepted by IGV? (.bam/.vcf)
4.2 years ago by WouterDeCoster 48k
1
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0
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1.6k
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Comment: Comment: Bioinformatics Definitions
4.2 years ago by WouterDeCoster 48k
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1
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2.5k
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Comment: Comment: how to align fastq files to a fasta file using biopython to produce VCF file
4.2 years ago by WouterDeCoster 48k
0
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1
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981
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Comment: Comment: Corset error
4.2 years ago by WouterDeCoster 48k
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1.3k
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Comment: Comment: extract the ids and key values
4.2 years ago by WouterDeCoster 48k
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3.0k
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Comment: Comment: How to search for genes 100Kb up and downstream of any genomic site
4.2 years ago by WouterDeCoster 48k
1
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0
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950
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Comment: Comment: What tools are best for conjoined gene/readthough detection and how do they diff
4.2 years ago by WouterDeCoster 48k
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1
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1.5k
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Comment: Comment: FeatureCounts Number of Reads
4.2 years ago by WouterDeCoster 48k
1
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0
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18k
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Comment: Comment: How to trim Nanopore reads. Please suggest a tool.
4.3 years ago by WouterDeCoster 48k
3
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1
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3.0k
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Answer: Answer: How to create a subset from a Nanopore fast5 file?
4.3 years ago by WouterDeCoster 48k
0
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0
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893
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Job: PhD position: bioinformatics analysis of omics data in frontotemporal dementia
genetics phd
updated 2.3 years ago by 45k • written 4.3 years ago by 48k
1
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1
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1.3k
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Comment: Comment: whole tissue and RNA-seq: can I still study specific cell types?
4.3 years ago by WouterDeCoster 48k
1
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1
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1.3k
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Comment: Comment: whole tissue and RNA-seq: can I still study specific cell types?
4.3 years ago by WouterDeCoster 48k
0
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1
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2.2k
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Comment: Comment: Hello everyone whenever i run this command this error terminates the command. ca
4.3 years ago by WouterDeCoster 48k
1
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2
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2.2k
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Comment: Comment: Hello everyone whenever i run this command this error terminates the command. ca
4.3 years ago by WouterDeCoster 48k
1
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1
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4.5k
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Comment: Comment: How to install argparse for python 2.7
4.3 years ago by WouterDeCoster 48k
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11k
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Comment: Comment: Change header of a Fasta file according to the file name
4.3 years ago by WouterDeCoster 48k
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1
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3.7k
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Comment: Comment: How to interpret a FASTA file
4.3 years ago by WouterDeCoster 48k
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0
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3.7k
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Comment: Comment: How to interpret a FASTA file
updated 4.3 years ago by 15k • written 4.3 years ago by 48k
2
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1
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4.3k
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Comment: Comment: Trimming on Nanopore Data
4.3 years ago by WouterDeCoster 48k
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1.0k
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Comment: Comment: How to use python to align 30 kb genome to another 30kb reference, repeat 10x ti
4.3 years ago by WouterDeCoster 48k
7,263 results • Page 3 of 146
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