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Comment: Comment: Filter BAM to keep only alignments at an interval, ignoring reads spliced over
27 days ago by WouterDeCoster 47k
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315
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Filter BAM to keep only alignments at an interval, ignoring reads spliced over
samtools bam splicing
27 days ago by WouterDeCoster 47k
2
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1
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971
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Answer: Answer: Is it possible to access the code of a bioinformatics article?
3 months ago by WouterDeCoster 47k
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559
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Comment: Comment: Find reference fasta based on M5/MD5 string
4 months ago by WouterDeCoster 47k
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559
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Comment: Comment: Find reference fasta based on M5/MD5 string
4 months ago by WouterDeCoster 47k
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854
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Comment: Comment: Isolating and extracting regions in VCF file
4 months ago by WouterDeCoster 47k
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4
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559
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Find reference fasta based on M5/MD5 string
reference fasta
4 months ago by WouterDeCoster 47k
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534
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Comment: Comment: Re-format sample columns in VCF file
4 months ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
4 months ago by WouterDeCoster 47k
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731
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Comment: Comment: somatic variant calling without matched normal in long-reads
4 months ago by WouterDeCoster 47k
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1
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1.1k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
4 months ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: ONT Raw Read Sequencing Pipeline
4 months ago by WouterDeCoster 47k
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1
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1.6k
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Comment: Comment: How to speed Salmon index up
4 months ago by WouterDeCoster 47k
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1.0k
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Comment: Comment: Snakemake rule error
5 months ago by WouterDeCoster 47k
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400
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Comment: Comment: how do I assemble centromere regions in a plant genome?
5 months ago by WouterDeCoster 47k
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358
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Comment: Comment: DOES MGI SEQUENCING RESULT CONTAINS MULTIPLE FILES FOR SINGLE SAMPLE
5 months ago by WouterDeCoster 47k
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2.5k
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Comment: Comment: How to remove fasta headers in a multifasta file and write file name as a fasta
8 months ago by WouterDeCoster 47k
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778
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Comment: Comment: Expected number of raw reads in fq.gz files in PE sequencing
8 months ago by WouterDeCoster 47k
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0
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277
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Number of reads per gene in pseudobulk with more or fewer nuclei
nuclei 10x sequencing
8 months ago by WouterDeCoster 47k
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1
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1.6k
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Comment: Comment: Create a reference genome from aligned bam file
8 months ago by WouterDeCoster 47k
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1
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1.4k
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Comment: Comment: Batch correction for Nanopore RNAseq
11 months ago by WouterDeCoster 47k
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725
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Comment: Comment: Extract samples from a VCF file that contain marker
11 months ago by WouterDeCoster 47k
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1
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640
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Answer: Answer: rust_htslib unrecognized filter ID
11 months ago by WouterDeCoster 47k
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626
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Answer: Answer: Truvari error: Failed to parse TBX_VCF - "ead mapping qualities">"
11 months ago by WouterDeCoster 47k
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489
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Comment: Comment: Pairwise Alignment
11 months ago by WouterDeCoster 47k
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1
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2.2k
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Comment: Comment: minimap's SAM file MAPQ value for the unique alignments
11 months ago by WouterDeCoster 47k
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621
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Comment: Comment: Colleges
11 months ago by WouterDeCoster 47k
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1
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904
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Answer: Answer: SyntaxError (Perhaps you forgot a comma?) in snakefile when running FastQC.
11 months ago by WouterDeCoster 47k
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819
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Comment: Comment: rna long read length distibution
12 months ago by WouterDeCoster 47k
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555
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Comment: Comment: Mapping reads to a multifasta reference
12 months ago by WouterDeCoster 47k
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1
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1.0k
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Comment: Comment: Estimate sizes of repeats in a especific Gene
12 months ago by WouterDeCoster 47k
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2.0k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
12 months ago by WouterDeCoster 47k
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1
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2.0k
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Comment: Comment: How to Diagnose Fragile X from Whole Genome Sequencing
12 months ago by WouterDeCoster 47k
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1.7k
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Comment: Comment: Nanopore config files
12 months ago by WouterDeCoster 47k
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1
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1.7k
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Answer: Answer: Nanopore config files
12 months ago by WouterDeCoster 47k
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0
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593
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Comment: Comment: Change VCF File Reference Genome to a Local .FA File
12 months ago by WouterDeCoster 47k
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1
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899
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Comment: Comment: problem with bedtools getfasta
13 months ago by WouterDeCoster 47k
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0
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842
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Answer: Answer: htseq-count : dosen't show options in bash ln ubuntu
13 months ago by WouterDeCoster 47k
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1.1k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
13 months ago by WouterDeCoster 47k
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0
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1.1k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
13 months ago by WouterDeCoster 47k
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1
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1.1k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
13 months ago by WouterDeCoster 47k
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1
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1.2k
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Comment: Comment: How can I generate VCF file with two different assembled genome fasta?
13 months ago by WouterDeCoster 47k
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1
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1.1k
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Comment: Comment: Genome sequenced [%] over time graph (Nanopore)
13 months ago by WouterDeCoster 47k
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0
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1.2k
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Comment: Comment: featureCounts problem in reading Gff
13 months ago by WouterDeCoster 47k
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1
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1.2k
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Comment: Comment: featureCounts problem in reading Gff
13 months ago by WouterDeCoster 47k
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0
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831
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Comment: Comment: Bioinformatics package
14 months ago by WouterDeCoster 47k
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0
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948
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Comment: Comment: Trying to make a Mauve alignment with 2 sequences and keep getting error code 3
14 months ago by WouterDeCoster 47k
2
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0
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575
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Answer: Answer: N50 value is equal to the single contig?
14 months ago by WouterDeCoster 47k
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2.4k
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Answer: Answer: long read + salmon? (transcript abundance)
14 months ago by WouterDeCoster 47k
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0
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6.4k
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Answer: Answer: Filtering out the spliced reads from bam file.
17 months ago by WouterDeCoster 47k
7,254 results • Page 1 of 146
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