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Comment: C: Fastq Trimmer by pattern
8.8 years ago by WouterDeCoster 48k
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3.5k
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Comment: C: Checking admixture with VCF and BAM files
8.8 years ago by WouterDeCoster 48k
1
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1
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3.5k
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Comment: C: Checking admixture with VCF and BAM files
8.8 years ago by WouterDeCoster 48k
0
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1
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3.5k
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Comment: C: Checking admixture with VCF and BAM files
8.8 years ago by WouterDeCoster 48k
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6.0k
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Comment: C: How to trim adapters and remove polyA tails from QuantSeq 3' FWD data
8.8 years ago by WouterDeCoster 48k
1
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0
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2.7k
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Comment: C: Shortest Missing K-mer
8.8 years ago by WouterDeCoster 48k
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4.0k
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Comment: C: How do you spend your time (productively) when your script is running?
8.8 years ago by WouterDeCoster 48k
1
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0
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4.0k
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Comment: C: How do you spend your time (productively) when your script is running?
8.8 years ago by WouterDeCoster 48k
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2
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4.0k
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Comment: C: How do you spend your time (productively) when your script is running?
8.8 years ago by WouterDeCoster 48k
1
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0
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4.0k
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Comment: C: How do you spend your time (productively) when your script is running?
8.8 years ago by WouterDeCoster 48k
3
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1
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4.0k
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Answer: A: How do you spend your time (productively) when your script is running?
8.8 years ago by WouterDeCoster 48k
2
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0
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1.8k
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Comment: C: Is this webserver trusted ??
8.8 years ago by WouterDeCoster 48k
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2.9k
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Comment: C: Determining sample size for co-expression analysis
8.8 years ago by WouterDeCoster 48k
1
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1
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2.3k
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Comment: C: RNA-Seq tophat comment error?
8.8 years ago by WouterDeCoster 48k
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0
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1.5k
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Comment: C: Biopython Entrez Query Record of IDs doesn't Match the Query Search Results
8.8 years ago by WouterDeCoster 48k
0
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0
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2.9k
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Comment: C: PCR Amplification necessity in RNASeq
8.8 years ago by WouterDeCoster 48k
0
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3.5k
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Comment: C: Fold Change accepts, FDR denies; which one to use ?
8.8 years ago by WouterDeCoster 48k
0
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0
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3.4k
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Comment: C: Where can i download the lncRNA expression profile for Lung adenocarcinoma
8.8 years ago by WouterDeCoster 48k
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1.7k
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Comment: C: Where i can get the sequence data of certain type of cancer mutation....?
8.8 years ago by WouterDeCoster 48k
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2.1k
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Comment: C: witch software is used to finde a mutation in the DNA sequencsing data. And what
8.8 years ago by WouterDeCoster 48k
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0
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3.1k
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Comment: C: Creating a targets matrix
8.8 years ago by WouterDeCoster 48k
1
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0
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2.1k
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Comment: C: witch software is used to finde a mutation in the DNA sequencsing data. And what
8.8 years ago by WouterDeCoster 48k
0
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1
reply
3.5k
views
Comment: C: Fold Change accepts, FDR denies; which one to use ?
8.8 years ago by WouterDeCoster 48k
0
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1
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3.5k
views
Comment: C: Fold Change accept, FDR deny; which one to use ?
8.8 years ago by WouterDeCoster 48k
1
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1
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3.5k
views
Comment: C: Fold Change accept, FDR deny; which one to use ?
8.8 years ago by WouterDeCoster 48k
1
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0
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2.9k
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Answer: A: is it ok to merge biological replicates for novel isoform discovery?
8.8 years ago by WouterDeCoster 48k
1
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0
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2.9k
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Comment: C: is it ok to merge biological replicates for novel isoform discovery?
8.8 years ago by WouterDeCoster 48k
1
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2
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3.5k
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Comment: C: Fold Change accept, FDR deny; which one to use ?
8.8 years ago by WouterDeCoster 48k
1
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0
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2.0k
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Comment: C: Best open source de novo assembler till date??
8.8 years ago by WouterDeCoster 48k
0
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0
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1.7k
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Comment: C: how to find the biological function of a protein complex ?
8.8 years ago by WouterDeCoster 48k
1
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1
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4.0k
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Comment: C: miRNA Target database?
8.8 years ago by WouterDeCoster 48k
1
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1
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2.7k
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Comment: C: GSEA - pathway analysis
8.8 years ago by WouterDeCoster 48k
0
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1
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6.4k
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Comment: C: diamond blastx always return error message "Insufficient arguments. Use diamond
8.8 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: modeling of large proteins
8.8 years ago by WouterDeCoster 48k
0
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1
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6.4k
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Comment: C: diamond blastx always return error message "Insufficient arguments. Use diamond
8.8 years ago by WouterDeCoster 48k
5
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1
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2.9k
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Answer: A: How to get gene full description with Ensembl IDs?
8.8 years ago by WouterDeCoster 48k
0
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0
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5.6k
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Comment: C: WGCNA error: Co-expression similarity and adjacency in Network Creation
8.8 years ago by WouterDeCoster 48k
0
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0
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4.2k
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Comment: C: Viral load estimation from WXS (whole exome sequencing) data
8.8 years ago by WouterDeCoster 48k
0
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0
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4.2k
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Comment: C: Viral load estimation from WXS (whole exome sequencing) data
8.8 years ago by WouterDeCoster 48k
0
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0
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4.2k
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Comment: C: Viral load estimation from WXS (whole exome sequencing) data
8.8 years ago by WouterDeCoster 48k
0
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1
reply
2.0k
views
Comment: C: Best open source de novo assembler till date??
8.8 years ago by WouterDeCoster 48k
0
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0
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3.2k
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Comment: C: How can I select my Chip-seq genes (targets) in my Rna-seq data?
8.8 years ago by WouterDeCoster 48k
1
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1
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15k
views
Comment: C: Pysam Fetching specified regions
8.8 years ago by WouterDeCoster 48k
0
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0
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1.8k
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Comment: C: How to install PANDAseq to cygwin?
8.8 years ago by WouterDeCoster 48k
0
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1
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15k
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Comment: C: Pysam Fetching specified regions
8.8 years ago by WouterDeCoster 48k
0
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1
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15k
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Comment: C: Pysam Fetching specified regions
8.8 years ago by WouterDeCoster 48k
0
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1
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15k
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Comment: C: Pysam Fetching specified regions
8.8 years ago by WouterDeCoster 48k
0
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0
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2.2k
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Comment: C: Split a BAM within a chromosome without losing read pairs
8.8 years ago by WouterDeCoster 48k
1
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0
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2.4k
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Answer: A: How to truncate the short reads to 30x coverage from 60x coverage
8.8 years ago by WouterDeCoster 48k
0
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1
reply
3.2k
views
Comment: C: How can I select my Chip-seq genes (targets) in my Rna-seq data?
8.8 years ago by WouterDeCoster 48k
7,263 results • Page 97 of 146
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