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Comment: Comment: No trimming of reverse reads using Trimmomatic-0.39
3.6 years ago by cpad0112 21k
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2.8k
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Comment: Comment: No trimming of reverse reads using Trimmomatic-0.39
3.6 years ago by cpad0112 21k
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2.9k
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Comment: Comment: ? in cram files
3.6 years ago by cpad0112 21k
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890
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Comment: Comment: Computational and experimental biology positions at University of Edinburgh - St
3.6 years ago by cpad0112 21k
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1.3k
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Comment: Comment: Snakemake error
3.6 years ago by cpad0112 21k
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1.3k
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Comment: Comment: How to extract reads which contain specific sequence from pair-end fastq files
3.6 years ago by cpad0112 21k
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0
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1.3k
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Comment: Comment: mono-allelic to bi-allelic (a unix tools question?)
3.6 years ago by cpad0112 21k
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1.2k
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Comment: Comment: The meaning of greter than character (>) in gene position in Genbank files
3.6 years ago by cpad0112 21k
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1
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1.3k
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Comment: Comment: mono-allelic to bi-allelic (a unix tools question?)
3.6 years ago by cpad0112 21k
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1.1k
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Comment: Comment: hgvs annotation from VCF
3.6 years ago by cpad0112 21k
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2.1k
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Comment: Comment: R - Merging and aligning two CSVs using common values in multiple columns
3.6 years ago by cpad0112 21k
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0
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735
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Comment: Comment: Add pvalues to multiple ggboxplots
3.6 years ago by cpad0112 21k
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1
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2.1k
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Comment: Comment: R - Merging and aligning two CSVs using common values in multiple columns
3.6 years ago by cpad0112 21k
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0
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2.1k
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Comment: Comment: R - Merging and aligning two CSVs using common values in multiple columns
3.6 years ago by cpad0112 21k
2
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1
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807
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Comment: Comment: R - Merging and aligning two CSVs using common values in multiple columns
3.6 years ago by cpad0112 21k
0
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0
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4.5k
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Comment: Comment: Use cat to sort multiple fastq files in a directory
3.6 years ago by cpad0112 21k
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0
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1.5k
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Comment: Comment: Open bioinformatics position in Emmanuelle Charpentier's lab
3.6 years ago by cpad0112 21k
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4.4k
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Comment: Comment: Convert 4 million SNPs' positions to rsID
3.6 years ago by cpad0112 21k
0
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1
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4.5k
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Comment: Comment: Use cat to sort multiple fastq files in a directory
3.6 years ago by cpad0112 21k
0
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1
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4.4k
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Comment: Comment: Convert 4 million SNPs' positions to rsID
3.6 years ago by cpad0112 21k
1
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1
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4.5k
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Comment: Comment: Use cat to sort multiple fastq files in a directory
3.6 years ago by cpad0112 21k
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0
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1.1k
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Comment: Comment: standalone blast error, stuck between two errors, i.e; query not accessible file
3.6 years ago by cpad0112 21k
1
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1
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1.4k
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Comment: Comment: Office computers on Windows
3.6 years ago by cpad0112 21k
1
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0
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1.2k
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Comment: Comment: Produce fasta file from genome coordinates
3.6 years ago by cpad0112 21k
1
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0
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1.4k
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Comment: Comment: How to output FASTQ file with four lines per sequence?
3.6 years ago by cpad0112 21k
0
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1
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1.4k
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Comment: Comment: How to output FASTQ file with four lines per sequence?
3.6 years ago by cpad0112 21k
1
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0
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15k
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Comment: Comment: Plotting overlapping lines in R
3.6 years ago by cpad0112 21k
2
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1
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2.3k
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Answer: Answer: sequence merge
3.6 years ago by cpad0112 21k
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0
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1.2k
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Comment: Comment: sequence renaming
3.6 years ago by cpad0112 21k
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1
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2.6k
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Comment: Comment: How to design one PCR primer for 5 different sequences by linux command line ?
3.6 years ago by cpad0112 21k
0
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1
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1.4k
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Comment: Comment: volcano plot of up and down genes into two parts, resprctively.
3.6 years ago by cpad0112 21k
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0
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7.6k
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Comment: Comment: Fasta File Python
3.6 years ago by cpad0112 21k
2
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2
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7.6k
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Comment: Comment: Fasta File Python
3.6 years ago by cpad0112 21k
1
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1
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7.6k
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Comment: Comment: Fasta File Python
3.6 years ago by cpad0112 21k
1
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1
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7.6k
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Comment: Comment: Fasta File Python
3.6 years ago by cpad0112 21k
1
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1
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2.9k
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Comment: Comment: how to query rsid's using dbsnp in r or linux
3.6 years ago by cpad0112 21k
0
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1
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3.7k
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Comment: Comment: how to run seqkit in a loop with multiple files
3.6 years ago by cpad0112 21k
1
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0
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3.7k
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Comment: Comment: how to run seqkit in a loop with multiple files
3.6 years ago by cpad0112 21k
1
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1
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3.1k
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Comment: Comment: Kallisto mapping paired end
3.6 years ago by cpad0112 21k
1
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1
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1.8k
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Comment: Comment: how to remove positions in VCF based on rsID
3.6 years ago by cpad0112 21k
0
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1
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1.8k
views
Comment: Comment: how to remove positions in VCF based on rsID
3.6 years ago by cpad0112 21k
1
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1
reply
3.1k
views
Comment: Comment: Kallisto mapping paired end
3.6 years ago by cpad0112 21k
1
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0
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898
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Answer: Answer: Trimming of reads
3.6 years ago by cpad0112 21k
0
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1
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1.7k
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Comment: Comment: Is there a tool that will tell me how "complex" (e.g., number of unique k-mers)
3.6 years ago by cpad0112 21k
0
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1
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3.7k
views
Comment: Comment: how to run seqkit in a loop with multiple files
3.6 years ago by cpad0112 21k
0
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1
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3.7k
views
Comment: Comment: how to run seqkit in a loop with multiple files
3.6 years ago by cpad0112 21k
1
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0
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1.6k
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Comment: Comment: How to use BCFtools to keep variants if they are `DP > 10` in all samples?
3.6 years ago by cpad0112 21k
2
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0
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3.7k
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Comment: Comment: FastQC for paired end data
3.6 years ago by cpad0112 21k
1
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1
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1.7k
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Comment: Comment: Is there a tool that will tell me how "complex" (e.g., number of unique k-mers)
3.6 years ago by cpad0112 21k
0
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0
replies
767
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Comment: Comment: Galaxy vs Cancer Genomics Cloud
3.6 years ago by cpad0112 21k
3,458 results • Page 7 of 70
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