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Comment: Comment: Why don't we align to pre-RNA for typical single-cell RNA-seq data? (CellRanger
2.2 years ago by Jeremy Leipzig 22k
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Comment: Comment: Error in executing STAR Aligner
2.3 years ago by Jeremy Leipzig 22k
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1.5k
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Comment: Comment: Error in executing STAR Aligner
2.3 years ago by Jeremy Leipzig 22k
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609
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Comment: Comment: does bioconductor/bioconductor_docker:RELEASE_X_Y install CRAN packages from a f
2.3 years ago by Jeremy Leipzig 22k
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11k
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Comment: Comment: How Much Does It Cost To Align A Flowcell In The Cloud?
2.3 years ago by Jeremy Leipzig 22k
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1.1k
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Comment: Comment: mirBase data to write a script to understand which is the dominant arm of a mirn
2.3 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: What are the pain points of using Genomics on the cloud today?
2.3 years ago by Jeremy Leipzig 22k
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1.1k
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Comment: Comment: mirBase data to write a script to understand which is the dominant arm of a mirn
2.3 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: Why there are symmetric splice junctions on IGV?
2.3 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: Why there are symmetric splice junctions on IGV?
2.3 years ago by Jeremy Leipzig 22k
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4.5k
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Comment: Comment: Is it possible to pass command line arguments to python script in snakemake?
2.3 years ago by Jeremy Leipzig 22k
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4.5k
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Comment: Comment: Is it possible to pass command line arguments to python script in snakemake?
2.3 years ago by Jeremy Leipzig 22k
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4.5k
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Comment: Comment: Is it possible to pass command line arguments to python script in snakemake?
2.3 years ago by Jeremy Leipzig 22k
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1.4k
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Comment: Comment: Snakemake issue
2.3 years ago by Jeremy Leipzig 22k
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1.8k
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Comment: Comment: Combining GTEx and TCGA data
2.4 years ago by Jeremy Leipzig 22k
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2.4k
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Comment: Comment: Percent identity in Blast
2.4 years ago by Jeremy Leipzig 22k
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2.1k
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Comment: Comment: How can NIH SRA data be more useful?
2.4 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: 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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1.9k
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Comment: Comment: Dragen-gatk for trio
2.4 years ago by Jeremy Leipzig 22k
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2.1k
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Comment: Comment: Why all those reads in bam files were unmapped?
2.4 years ago by Jeremy Leipzig 22k
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4.3k
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Comment: Comment: multiqc could not generate results
2.4 years ago by Jeremy Leipzig 22k
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2.2k
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Comment: Comment: How to bechmark a human dataset ? (is it needed)
2.5 years ago by Jeremy Leipzig 22k
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639
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Comment: Comment: Extremely large fold change for miRNA differential expression analysis
2.5 years ago by Jeremy Leipzig 22k
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681
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Comment: Comment: Is it correct to merge multiple gvcf from separate variant calling?
2.5 years ago by Jeremy Leipzig 22k
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7.6k
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Comment: Comment: Is there ever a good reason to use a log transformation instead of Box-Cox?
2.5 years ago by Jeremy Leipzig 22k
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2.3k
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Comment: Comment: troubleshooting benchmarking small variants: hap.py and rtg
2.5 years ago by Jeremy Leipzig 22k
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781
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Comment: Comment: Stool miRNA - low alignment rate
2.6 years ago by Jeremy Leipzig 22k
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3.3k
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Comment: Comment: Difference between Genotype 0|1 and 1|0 in VCF file?
2.6 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: Why my reads mapping rate extremely low
2.6 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: Merging of RNA-seq datasets from different studies
2.6 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: Merging of RNA-seq datasets from different studies
2.6 years ago by Jeremy Leipzig 22k
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806
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Comment: Comment: Tools or Method for batch analysis of Paired end WES data in a queue way.
2.6 years ago by Jeremy Leipzig 22k
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1.8k
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Comment: Comment: comparing variants between two VCF files
2.7 years ago by Jeremy Leipzig 22k
1
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707
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Comment: Comment: best tool for the pipeline wrapper
2.7 years ago by Jeremy Leipzig 22k
1
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1
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2.2k
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Comment: Comment: Snakemake bwa mem
2.7 years ago by Jeremy Leipzig 22k
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1.8k
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Comment: Comment: Rshiny - ggplot - density plot
2.7 years ago by Jeremy Leipzig 22k
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1.8k
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Comment: Comment: Rshiny - ggplot - density plot
2.7 years ago by Jeremy Leipzig 22k
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1.6k
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Comment: Comment: STAR vs Novoalign IGV Browser visualization
2.7 years ago by Jeremy Leipzig 22k
2
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822
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Comment: Comment: What Galaxy tools add Ns to variable length FASTQ sequences to get uniform lengt
2.8 years ago by Jeremy Leipzig 22k
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1.8k
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Comment: Comment: Bioinformatics
2.9 years ago by Jeremy Leipzig 22k
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3.3k
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Comment: Comment: Looping over a function in R, and needing a variable name to save output as uniq
2.9 years ago by Jeremy Leipzig 22k
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5.8k
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Comment: Comment: convert VCF to gVCF
2.9 years ago by Jeremy Leipzig 22k
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1
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2.1k
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Comment: Comment: snakemake job status monitoring
2.9 years ago by Jeremy Leipzig 22k
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1
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2.3k
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Comment: Comment: troubleshooting benchmarking small variants: hap.py and rtg
2.9 years ago by Jeremy Leipzig 22k
0
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1
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766
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Comment: Comment: Best method of integrative analysis for GWAS and differential expression data
2.9 years ago by Jeremy Leipzig 22k
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868
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Comment: Comment: Very low number of micro RNA reads
2.9 years ago by Jeremy Leipzig 22k
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1.1k
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Comment: Comment: How to combine datasets from different sequencing platforms?
3.0 years ago by Jeremy Leipzig 22k
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2.5k
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Comment: Comment: What are the pain points in genomic variant interpretation/annotation processes?
3.0 years ago by Jeremy Leipzig 22k
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2.3k
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Comment: Comment: troubleshooting benchmarking small variants: hap.py and rtg
3.0 years ago by Jeremy Leipzig 22k
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1
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2.3k
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Comment: Comment: troubleshooting benchmarking small variants: hap.py and rtg
3.0 years ago by Jeremy Leipzig 22k
816 results • Page 4 of 17
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