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Answer: Answer: SNPEff - Exonic Variants
16 months ago by Jeremy Leipzig 22k
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26k
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Answer: Answer: Best way to query VCF for specific variants
18 months ago by Jeremy Leipzig 22k
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1.8k
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Answer: Answer: Confused about which database to use - nt or nr?
19 months ago by Jeremy Leipzig 22k
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523
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Answer: Answer: How to calculate how many identical elements are in each line of a file
19 months ago by Jeremy Leipzig 22k
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2.4k
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Answer: Answer: Set up a blast remote server
19 months ago by Jeremy Leipzig 22k
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2.6k
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Answer: Answer: Can bioinformatics Phds be completely or almost completely done remotely?
19 months ago by Jeremy Leipzig 22k
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1.7k
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Answer: Answer: r script is not working in snakemake
20 months ago by Jeremy Leipzig 22k
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1.2k
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Answer: Answer: difference between different field info in vcf file format
20 months ago by Jeremy Leipzig 22k
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4.2k
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Answer: Answer: How to merge many huge gVCFs with high speed.
20 months ago by Jeremy Leipzig 22k
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1.7k
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Answer: Answer: How to get intersected variants between multiple vcf files?
20 months ago by Jeremy Leipzig 22k
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636
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Answer: Answer: What are the biggest sets of individual-level sequence-based variant data?
22 months ago by Jeremy Leipzig 22k
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814
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Answer: Answer: Error when trying to make MetaXcan run through Snakemake
23 months ago by Jeremy Leipzig 22k
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828
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Answer: Answer: huge difference when comparing 2 vcf files from the same sample
2.0 years ago by Jeremy Leipzig 22k
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491
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Answer: Answer: How to download NGS-based raw data from GTEx database
2.0 years ago by Jeremy Leipzig 22k
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1
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1.5k
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Answer: Answer: Error in executing STAR Aligner
2.2 years ago by Jeremy Leipzig 22k
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1.6k
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Answer: Answer: Trimmomatic seems not working
2.2 years ago by Jeremy Leipzig 22k
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566
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Answer: Answer: Variant calling
2.2 years ago by Jeremy Leipzig 22k
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1
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862
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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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553
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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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733
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Answer: Answer: The Biostar Herald for Monday, January 03, 2022
2.3 years ago by Jeremy Leipzig 22k
4
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3
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2.1k
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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
3
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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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760
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Answer: Answer: Merging genotyping array VCFs and then running kinship analysis
2.4 years ago by Jeremy Leipzig 22k
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893
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Answer: Answer: Snakemake restricted wildcard combinations
2.4 years ago by Jeremy Leipzig 22k
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1
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907
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Answer: Answer: error while annotating vcf file using snpEff
2.4 years ago by Jeremy Leipzig 22k
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954
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Answer: Answer: How can I know what is a good and bad variant call?
2.4 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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4.9k
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Answer: Answer: Using AWS for Bioinformatics
2.5 years ago by Jeremy Leipzig 22k
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0
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974
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Answer: Answer: Human Exome Variant Reference
2.5 years ago by Jeremy Leipzig 22k
4
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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
2.5 years ago by Jeremy Leipzig 22k
2
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0
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578
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Answer: Answer: How to get list of all approved Antibiotics
2.6 years ago by Jeremy Leipzig 22k
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1.7k
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Answer: Answer: comparing variants between two VCF files
2.6 years ago by Jeremy Leipzig 22k
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1.3k
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Answer: Answer: Validation of somatic variant calling pipeline
2.7 years ago by Jeremy Leipzig 22k
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1.6k
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Answer: Answer: Change STAR Parameters in rsem-calculate-expression
2.7 years ago by Jeremy Leipzig 22k
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0
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917
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Answer: Answer: ClinicalTrial data in CSV format
2.8 years ago by Jeremy Leipzig 22k
1
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1.3k
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Answer: Answer: GATK joint genotyping
2.8 years ago by Jeremy Leipzig 22k
1
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1
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1.8k
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Answer: Answer: Bioinformatics
2.8 years ago by Jeremy Leipzig 22k
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0
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867
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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
2.9 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
2.9 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
1
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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
3.0 years ago by Jeremy Leipzig 22k
1
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0
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735
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Answer: Answer: Interested in benchmarks? Please take our survey!
3.0 years ago by Jeremy Leipzig 22k
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0
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2.0k
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Answer: Answer: how to run and use the ENCODE ATAC-seq pipline
3.0 years ago by Jeremy Leipzig 22k
3
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0
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42k
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Answer: Answer: Any Good Bam And Sam Viewer?
3.1 years ago by Jeremy Leipzig 22k
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2.2k
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Answer: Answer: Remap GRCh38.p13 to GRCh38
3.1 years ago by Jeremy Leipzig 22k
2
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3
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2.1k
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Answer: Answer: What are the necessary and sufficient conditions for applying a multiple hypothe
3.1 years ago by Jeremy Leipzig 22k
421 results • Page 2 of 9
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