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Answer:
A: Why don't phylogenetic analyses using DNA sequences and protein sequences result
7.4 years ago by
DG
7.3k
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Answer:
A: bcftools isec: weird number of output file
7.4 years ago by
DG
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Answer:
A: Threshold to exclude samples based on sample-to-sample distances
7.5 years ago by
DG
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Answer:
A: genes in RAS/MEK pathway
7.5 years ago by
DG
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Answer:
A: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by
DG
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Answer:
A: Is there an over representation for cancer processes in pathway databases (e.g.
7.7 years ago by
DG
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Answer:
A: VariantCalling with single sanger read
7.7 years ago by
DG
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Answer:
A: Cancer DNA sequences
7.7 years ago by
DG
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Answer:
A: How to check new variants for functional effects?
7.7 years ago by
DG
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Answer:
A: Determining Pearson correlation coefficients and significance (p-value) for miRN
7.8 years ago by
DG
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Answer:
A: I want to store a docker image reproducing a paper. Is there a host for docker i
7.8 years ago by
DG
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Answer:
A: How to estimate whether more than one copy of a gene is mutated?
7.8 years ago by
DG
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Answer:
A: Determine whether a gene is totally missing
7.8 years ago by
DG
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Answer:
A: Tool for calculating variant frequency
7.8 years ago by
DG
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Answer:
A: Load MSA text from FluDB into Excel
7.8 years ago by
DG
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Answer:
A: What is the "Amino Acid substitution rate"?
7.8 years ago by
DG
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Answer:
A: gene prediction using gene/protein sequence from a closely related species, both
7.8 years ago by
DG
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Answer:
A: What training do you think a computer scientist should do to move into the bioin
7.9 years ago by
DG
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Answer:
A: NGS storage on AWS S3
7.9 years ago by
DG
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Answer:
A: What is best commercial software for exome/genome interpretation?
7.9 years ago by
DG
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Answer:
A: Cuffmerge:Which samples to use for creating a merged gtf file?
7.9 years ago by
DG
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Answer:
A: difficulty in underestanding terms and graphs
7.9 years ago by
DG
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Answer:
A: COmparing two SNV vcf files using bedtools
7.9 years ago by
DG
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Answer:
A: Amplicons assembly/aligning method to find its targets?
7.9 years ago by
DG
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1.8k
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Answer:
A: Variant calling with multi samples using RNASeq
7.9 years ago by
DG
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4.0k
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Answer:
A: Correct for batch-effects which are not visible in pca-plot of raw-data (RNA-Seq
7.9 years ago by
DG
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Answer:
A: raw data information about genetic data?
8.0 years ago by
DG
7.3k
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Answer:
A: Extracting heterozygous genotype from vcf file and compare 2 files
8.0 years ago by
DG
7.3k
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Answer:
A: Help selecting storage hardware for bioinformatics core facilities
8.0 years ago by
DG
7.3k
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Answer:
A: Duplicates in Whole Exome Sequence Data
8.0 years ago by
DG
7.3k
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2.7k
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Answer:
A: Bwa mem is giving me alignements that are causing noise in subsequent analysis.
8.0 years ago by
DG
7.3k
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Answer:
A: Removing gaps from a multiple sequence alignment in order to analyse SNPs
8.0 years ago by
DG
7.3k
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4.5k
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Answer:
A: Quantum Bioinformatics ahead?
8.0 years ago by
DG
7.3k
2
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2.1k
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Answer:
A: Next Generation Sequencing Pipeline
8.0 years ago by
DG
7.3k
5
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3.0k
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Answer:
A: Difference between somatic mutations and somatic hyper mutation
8.0 years ago by
DG
7.3k
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Answer:
A: Terminologies about hyper mutation
8.0 years ago by
DG
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Answer:
A: VCF - compare
8.1 years ago by
DG
7.3k
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3.7k
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Answer:
A: ClinVar local install
8.1 years ago by
DG
7.3k
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Answer:
A: What's the maximum number of threads that bwa mem can handle?
8.1 years ago by
DG
7.3k
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1.5k
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Answer:
A: Classifying proteins as enzymes, GPCRs, ion channels, etc.
8.1 years ago by
DG
7.3k
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Answer:
A: How to separate germline variants from somatic and vice-versa in cancer
8.1 years ago by
DG
7.3k
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2.8k
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Answer:
A: annotating Multiple Phylogenetic trees on the basis of color
8.1 years ago by
DG
7.3k
3
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4.2k
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Answer:
A: about somatic mutation calling
8.1 years ago by
DG
7.3k
2
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5.5k
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Answer:
A: Targeted NGS: amplicon length vs read length
8.1 years ago by
DG
7.3k
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5.0k
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Answer:
A: GATK MuTect2 duplication filter
8.1 years ago by
DG
7.3k
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5.1k
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Answer:
A: BSc Computer Science dissertation project ideas
8.1 years ago by
DG
7.3k
0
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2.4k
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Answer:
A: VarDictJava BED file input Problem
8.1 years ago by
DG
7.3k
0
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3.8k
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Answer:
A: How to determine if an amino acid is part of a-helix or B-sheet in pdb file
8.1 years ago by
DG
7.3k
1
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1
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1.6k
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Answer:
A: need a database for Variants with less freq than SNPs
8.2 years ago by
DG
7.3k
2
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0
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5.4k
views
Answer:
A: How to creat a phylogenetic tree for SPECIES?
8.2 years ago by
DG
7.3k
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