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Comment: Where to find known sites for mm39 used by GATK4 BaseRecalibrator?
2.0 years ago by
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C: Is there a tool to find the correct percentage of duplication levels in FastQ ?
3.8 years ago by
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C: Is there a tool to find the correct percentage of duplication levels in FastQ ?
3.9 years ago by
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C: Is there a tool to find the correct percentage of duplication levels in FastQ ?
3.9 years ago by
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C: Is there a tool to find the correct percentage of duplication levels in FastQ ?
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C: Is there a tool to find the correct percentage of duplication levels in FastQ ?
3.9 years ago by
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C: Is it possible to get the Codons for an intron/splice mutation given the chromos
3.9 years ago by
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C: Is it possible to get convert all NC_ to NP_ for RefSeq ?
4.0 years ago by
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C: Is it possible to get convert all NC_ to NP_ for RefSeq ?
4.0 years ago by
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C: Is it possible to obtain all the RefSeq transcripts of Ensembl genes for GRCh37
4.3 years ago by
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C: Is it possible to obtain all the RefSeq transcripts of Ensembl genes for GRCh37
4.3 years ago by
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C: Is it possible to obtain all the RefSeq transcripts of Ensembl genes for GRCh37
4.3 years ago by
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C: Is it possible to output uncompressed FastQ files with bcl2fastq2 ?
4.8 years ago by
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C: Is it possible to output uncompressed FastQ files with bcl2fastq2 ?
4.8 years ago by
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C: Should the expression data be centered before PCA?
4.8 years ago by
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C: Is it possible to output uncompressed FastQ files with bcl2fastq2 ?
4.8 years ago by
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C: Is it possible to output uncompressed FastQ files with bcl2fastq2 ?
4.8 years ago by
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C: RNA-seq: is there a way to get the variability between biological replicates ?
5.1 years ago by
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C: RNA-seq: is there a way to get the variability between biological replicates ?
5.1 years ago by
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C: RNA-seq: is there a way to get the variability between biological replicates ?
5.1 years ago by
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C: RNA-seq: is there a way to get the variability between biological replicates ?
5.1 years ago by
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C: RNA-seq: Is it worth to analyze case vs control separately to have a % similarit
5.1 years ago by
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C: RNA-seq: Is it worth to analyze case vs control separately to have a % similarit
5.1 years ago by
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C: RNA-seq: Is it worth to analyze case vs control separately to have a % similarit
5.1 years ago by
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C: RNA-seq: Is it worth to analyze case vs control separately to have a % similarit
5.1 years ago by
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C: RNA-seq: Is it worth to analyze case vs control separately to have a % similarit
5.1 years ago by
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C: RNA-seq: Is it worth to analyze case vs control separately to have a % similarit
5.1 years ago by
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C: What does CSQ means in a VCF file annotated by VEP ?
5.2 years ago by
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C: MySQL: Mapping GRCh38 coordinates to GRCh37 using ensembldb
5.3 years ago by
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C: bcl2fastq2: how to correctly use the --use-bases-mask for different sequencing m
5.5 years ago by
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Comment:
C: Using Circos plot to visualize RNA-seq data
5.8 years ago by
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Comment:
C: Using Circos plot to visualize RNA-seq data
5.8 years ago by
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Comment:
C: Using Circos plot to visualize RNA-seq data
5.8 years ago by
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Comment:
C: HTSeq-count [Python] is not properly counting reads like Genomic Alignments [R]
5.9 years ago by
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C: HTSeq-count [Python] is not properly counting reads like Genomic Alignments [R]
5.9 years ago by
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Comment:
C: TCGA calling pipeline query
6.1 years ago by
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C: Overlap of variants between CaVEMan and MuTect2 ?
6.1 years ago by
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C: [solved] SnpEff reports intron variants in exons ?
6.6 years ago by
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Comment:
C: SnpEff reports intron variants in exons ?
6.6 years ago by
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Comment:
C: SnpEff reports intron variants in exons ?
6.6 years ago by
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Comment:
C: Intersection of a BED genes with multiple VCFs: report only if at least N inters
7.0 years ago by
乙
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