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Answer: Answer: Average number of homozygous SNVs in WGS
16 months ago by Jeremy Leipzig 22k
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702
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Answer: Answer: Reference mitochondrial DNA in GRCh37
17 months ago by Jeremy Leipzig 22k
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1.1k
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Answer: Answer: Availability of information on genes in Gnomad VCF data
17 months ago by Jeremy Leipzig 22k
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1.2k
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Answer: Answer: SNPEff - Exonic Variants
17 months ago by Jeremy Leipzig 22k
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27k
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Answer: Answer: Best way to query VCF for specific variants
19 months ago by Jeremy Leipzig 22k
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2.0k
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Answer: Answer: Confused about which database to use - nt or nr?
20 months ago by Jeremy Leipzig 22k
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538
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Answer: Answer: How to calculate how many identical elements are in each line of a file
20 months ago by Jeremy Leipzig 22k
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2.5k
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Answer: Answer: Set up a blast remote server
20 months ago by Jeremy Leipzig 22k
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2.7k
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Answer: Answer: Can bioinformatics Phds be completely or almost completely done remotely?
20 months ago by Jeremy Leipzig 22k
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1.8k
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Answer: Answer: r script is not working in snakemake
21 months ago by Jeremy Leipzig 22k
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1.3k
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Answer: Answer: difference between different field info in vcf file format
21 months ago by Jeremy Leipzig 22k
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4.3k
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Answer: Answer: How to merge many huge gVCFs with high speed.
21 months ago by Jeremy Leipzig 22k
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1.8k
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Answer: Answer: How to get intersected variants between multiple vcf files?
21 months ago by Jeremy Leipzig 22k
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653
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Answer: Answer: What are the biggest sets of individual-level sequence-based variant data?
23 months ago by Jeremy Leipzig 22k
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842
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Answer: Answer: Error when trying to make MetaXcan run through Snakemake
24 months ago by Jeremy Leipzig 22k
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862
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Answer: Answer: huge difference when comparing 2 vcf files from the same sample
2.1 years ago by Jeremy Leipzig 22k
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503
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Answer: Answer: How to download NGS-based raw data from GTEx database
2.1 years ago by Jeremy Leipzig 22k
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1.5k
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Answer: Answer: Error in executing STAR Aligner
2.3 years ago by Jeremy Leipzig 22k
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1.6k
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Answer: Answer: Trimmomatic seems not working
2.3 years ago by Jeremy Leipzig 22k
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579
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Answer: Answer: Variant calling
2.3 years ago by Jeremy Leipzig 22k
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897
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Answer: Answer: The Biostar Herald for Monday, January 24, 2022
2.3 years ago by Jeremy Leipzig 22k
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566
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Answer: Answer: Does software significantly impact fold change values?
2.3 years ago by Jeremy Leipzig 22k
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743
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Answer: Answer: The Biostar Herald for Monday, January 03, 2022
2.4 years ago by Jeremy Leipzig 22k
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2.2k
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Answer: Answer: How can NIH SRA data be more useful?
2.4 years ago by Jeremy Leipzig 22k
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1.4k
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Answer: Answer: QC with RNA-SeQC output weird
2.4 years ago by Jeremy Leipzig 22k
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1.6k
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Answer: Answer: Why isn't it a common practice to call variant for every position in human genom
2.4 years ago by Jeremy Leipzig 22k
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778
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Answer: Answer: Merging genotyping array VCFs and then running kinship analysis
2.5 years ago by Jeremy Leipzig 22k
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920
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Answer: Answer: Snakemake restricted wildcard combinations
2.5 years ago by Jeremy Leipzig 22k
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929
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Answer: Answer: error while annotating vcf file using snpEff
2.5 years ago by Jeremy Leipzig 22k
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0
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974
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Answer: Answer: How can I know what is a good and bad variant call?
2.5 years ago by Jeremy Leipzig 22k
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1.1k
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Answer: Answer: Question for Splice variants and Alternative splicing
2.5 years ago by Jeremy Leipzig 22k
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5.1k
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Answer: Answer: Using AWS for Bioinformatics
2.6 years ago by Jeremy Leipzig 22k
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0
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1.0k
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Answer: Answer: Human Exome Variant Reference
2.6 years ago by Jeremy Leipzig 22k
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2.2k
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Answer: Answer: How to bechmark a human dataset ? (is it needed)
2.5 years ago by Jeremy Leipzig 22k
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1
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1.2k
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Answer: Answer: How does one map between drugbank ids and rxnorm ids (ids used in TWOSIDES and O
2.6 years ago by Jeremy Leipzig 22k
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0
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589
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Answer: Answer: How to get list of all approved Antibiotics
2.7 years ago by Jeremy Leipzig 22k
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0
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1.8k
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Answer: Answer: comparing variants between two VCF files
2.7 years ago by Jeremy Leipzig 22k
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1.3k
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Answer: Answer: Validation of somatic variant calling pipeline
2.8 years ago by Jeremy Leipzig 22k
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1.7k
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Answer: Answer: Change STAR Parameters in rsem-calculate-expression
2.8 years ago by Jeremy Leipzig 22k
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0
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935
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Answer: Answer: ClinicalTrial data in CSV format
2.9 years ago by Jeremy Leipzig 22k
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0
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1.3k
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Answer: Answer: GATK joint genotyping
2.9 years ago by Jeremy Leipzig 22k
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1
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1.8k
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Answer: Answer: Bioinformatics
2.9 years ago by Jeremy Leipzig 22k
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0
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882
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Answer: Answer: Lukemia
2.9 years ago by Jeremy Leipzig 22k
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0
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12k
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Answer: Answer: Basic Bam File Annotation
3.0 years ago by Jeremy Leipzig 22k
1
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1
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1.9k
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Answer: Answer: Snakemake wildcards in the path input/output
3.0 years ago by Jeremy Leipzig 22k
2
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1
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2.6k
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Answer: Answer: Snakemake and STARsolo
3.0 years ago by Jeremy Leipzig 22k
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3
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1.2k
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Answer: Answer: RefSeq Annotation Report - Gene and Feature Statistics
3.0 years ago by Jeremy Leipzig 22k
2
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2
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1.9k
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Answer: Answer: Using snakemake in order to download reads and run hisat2 mapping
3.1 years ago by Jeremy Leipzig 22k
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0
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741
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Answer: Answer: Interested in benchmarks? Please take our survey!
3.1 years ago by Jeremy Leipzig 22k
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2.0k
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Answer: Answer: how to run and use the ENCODE ATAC-seq pipline
3.1 years ago by Jeremy Leipzig 22k
424 results • Page 2 of 9
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