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Answer: A: Sizes of Nanopore files and how to store?
4.1 years ago by WouterDeCoster 47k
0
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0
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8.9k
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Answer: A: Memory error in python
4.1 years ago by WouterDeCoster 47k
0
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1
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1.5k
views
Answer: A: fastqc duplicate reads
4.2 years ago by WouterDeCoster 47k
3
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1
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2.2k
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Answer: A: Current challenges in SARS-CoV-2 analysis?
4.2 years ago by WouterDeCoster 47k
2
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1
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1.4k
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Answer: A: Book recommendation for starting and advancing in Bioinformatics
4.2 years ago by WouterDeCoster 47k
1
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0
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798
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Answer: A: Transferring Phase information from one VCF to another
4.2 years ago by WouterDeCoster 47k
1
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1
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1.6k
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Answer: A: Multiple mapping with longreads - Get primary mapping
4.2 years ago by WouterDeCoster 47k
3
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3
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6.1k
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Answer: A: bcftools merge 1021 individual vcf files
4.2 years ago by WouterDeCoster 47k
0
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1
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3.2k
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Answer: A: Assembly of oxford nanopore sequencing data
4.2 years ago by WouterDeCoster 47k
1
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1
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2.8k
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Answer: A: Question regarding journal publications
4.2 years ago by WouterDeCoster 47k
2
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2
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3.1k
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Answer: A: ONT fast5 basecalling
4.2 years ago by WouterDeCoster 47k
3
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1
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2.5k
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Answer: A: Ru/Read Until in Nanopore sequencers
4.2 years ago by WouterDeCoster 47k
2
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0
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1.1k
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Answer: A: Nanopolish variant calling. Need to specify input region of the reference genome
4.3 years ago by WouterDeCoster 47k
2
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0
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1.0k
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Answer: A: merge CNV calls from different softwares
4.3 years ago by WouterDeCoster 47k
0
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1
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1.2k
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Answer: A: Trimming of fasta file headers
4.3 years ago by WouterDeCoster 47k
0
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0
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864
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Answer: A: How convert a fastQ file to a Sam/Bam file
4.3 years ago by WouterDeCoster 47k
1
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1
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712
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Answer: A: Denovo sequencing of species in different locations
4.3 years ago by WouterDeCoster 47k
4
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1
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2.7k
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Answer: A: Should I keep up with random contigs in human genome
4.3 years ago by WouterDeCoster 47k
1
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1
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1.3k
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Answer: A: DEseq2 tool on Galaxy software problems regarding normalization of featurecounts
4.3 years ago by WouterDeCoster 47k
1
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0
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1.4k
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Answer: C: Haplotypecaller indel realignment
4.3 years ago by WouterDeCoster 47k
3
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0
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6.3k
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Answer: A: Variant calling on Nanopore reads
4.3 years ago by WouterDeCoster 47k
1
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1
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2.6k
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Answer: A: Sanger sequencing data analysis
4.4 years ago by WouterDeCoster 47k
1
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1
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1.3k
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Answer: A: Mimick WES on WGS data + A comprehensive list of coding regions in the most biol
4.4 years ago by WouterDeCoster 47k
6
votes
0
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8.0k
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Answer: A: gatk4 GenomicsDBImport intervals with whole genome
4.4 years ago by WouterDeCoster 47k
4
votes
3
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799
views
Answer: C: RNA seq query
4.4 years ago by WouterDeCoster 47k
1
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1
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2.9k
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Answer: A: Interesting things to do with 23andme data
4.5 years ago by WouterDeCoster 47k
0
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0
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1.3k
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Answer: A: nanopor reads analysis using nanoplot
4.5 years ago by WouterDeCoster 47k
4
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1
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1.3k
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Answer: A: Mapping whole exome sequencing
4.5 years ago by WouterDeCoster 47k
3
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0
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3.3k
views
Answer: A: Concatenate fastq files before or after trimming?
4.5 years ago by WouterDeCoster 47k
2
votes
0
replies
1.2k
views
Answer: A: How to extract a particular region from a nucleotide contig?
4.5 years ago by WouterDeCoster 47k
3
votes
2
replies
1.8k
views
Answer: A: Whole genome sequencing or whole exome sequencing- which is better and why?
4.5 years ago by WouterDeCoster 47k
1
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1
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2.0k
views
Answer: C: Error converting from the ENTREZ GENE ID to GENE SYMBOLS
4.5 years ago by WouterDeCoster 47k
4
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1
reply
2.1k
views
Answer: A: How I do a loop over multiple files in terminal?
4.5 years ago by WouterDeCoster 47k
2
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1
reply
6.0k
views
Answer: A: loading yaml file into snakemake
4.5 years ago by WouterDeCoster 47k
7
votes
1
reply
2.2k
views
Answer: A: What is in your opinion the current state-of-the-art sequencing platform for gen
4.5 years ago by WouterDeCoster 47k
5
votes
0
replies
1.8k
views
Answer: A: Prioritizing structural variants and CNV
4.6 years ago by WouterDeCoster 47k
1
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1
reply
2.5k
views
Answer: C: DEXSeq Installation Error
4.6 years ago by WouterDeCoster 47k
1
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2
replies
952
views
Answer: A: Reconstruct reference sequence from SAM file?
4.6 years ago by WouterDeCoster 47k
0
votes
1
reply
2.1k
views
Answer: A: Aligning multiple Fastq files using Bowtie2
4.6 years ago by WouterDeCoster 47k
1
vote
1
reply
580
views
Answer: A: API for searching for adjacent genes
4.6 years ago by WouterDeCoster 47k
1
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0
replies
1.7k
views
Answer: C: Installation error - RNAPLEX
4.6 years ago by WouterDeCoster 47k
0
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0
replies
2.5k
views
Answer: A: [W::bcf_hdr_check_sanity] GL should be declared as Number=G
4.6 years ago by WouterDeCoster 47k
1
vote
0
replies
2.3k
views
Answer: A: hg19 exon, intron, UTR region
4.6 years ago by WouterDeCoster 47k
3
votes
1
reply
2.0k
views
Answer: C: How to properly measure the length of a reference genome
4.6 years ago by WouterDeCoster 47k
2
votes
0
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3.5k
views
Answer: A: How do I install the R package on GitHub with bioconda
4.6 years ago by WouterDeCoster 47k
2
votes
2
replies
833
views
Answer: A: How to get the extended flanking read sequences in the reference based genome as
4.6 years ago by WouterDeCoster 47k
3
votes
0
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1.1k
views
Answer: A: Can I combine RPM values of RNA datasets from tow different databases?
4.6 years ago by WouterDeCoster 47k
2
votes
1
reply
2.6k
views
Answer: A: Getting and empty .fastq file as output when ran poretools command on multiple .
4.6 years ago by WouterDeCoster 47k
1
vote
0
replies
982
views
Answer: A: Plenty of gaps with my sam alignment file, why is that?
4.7 years ago by WouterDeCoster 47k
2
votes
0
replies
767
views
Answer: A: Assembly of DNA from .bam file
4.7 years ago by WouterDeCoster 47k
982 results • Page 2 of 20
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