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Comment: Comment: why there is many broken paired reads in my Illumina reads and how to solve them
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
0
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8.4k
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Comment: Comment: why there is many broken paired reads in my Illumina reads and how to solve them
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
5
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2
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7.3k
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Comment: Comment: hello I know I must accept that im a stupid
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
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Comment: Comment: how to retreive sequences given a start and end site.
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
2
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4.6k
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Answer: Answer: TO BLAST LARGE QUERY SEQUENCE AT ONE TIME
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
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2
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6.6k
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Comment: Comment: convert SOLID color space to base-space
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
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6.6k
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Comment: Comment: convert SOLID color space to base-space
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
0
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1
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6.6k
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Comment: Comment: convert SOLID color space to base-space
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
0
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1
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5.0k
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Comment: Comment: Perplexing Bowtie 2 results
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
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0
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5.0k
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Comment: Comment: How to find the diversity of nucleotides in each position of an alignment ?
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
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1
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5.0k
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Comment: Comment: Perplexing Bowtie 2 results
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
4
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1
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5.0k
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Answer: Answer: Perplexing Bowtie 2 results
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
1
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0
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5.0k
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Comment: C: Perplexing Bowtie 2 results
11.0 years ago by Ashutosh Pandey 12k
0
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1
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5.0k
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Comment: Comment: Perplexing Bowtie 2 results
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
0
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1
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2.8k
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Answer: Answer: Bioawk: multiple criteria
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
2
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13k
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Comment: C: I want to re-open the old debate: python or perl ?
11.0 years ago by Ashutosh Pandey 12k
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12k
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Comment: Comment: How to generate a .sam/.bam file of a particular chromosome or even a particular
updated 3.7 years ago by 45k • written 11.0 years ago by 12k
5
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3
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12k
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Answer: Answer: How to generate a .sam/.bam file of a particular chromosome or even a particular
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
1
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0
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4.8k
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Comment: Comment: Second column in Ensembl GTF: source or biotype?
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
0
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1
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4.8k
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Comment: Comment: Second column in Ensembl GTF: source or biotype?
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
2
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0
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11k
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Answer: Answer: fastx toolkit problem: fastq to fasta
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
3
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5.8k
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Answer: Answer: Computational infrastructure required for RNAseq analysis, genome annotation and
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
0
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0
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7.8k
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Comment: Comment: Ensembl VEP filtering most_severe keeping Symbol, Feature,Consequence etc.
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
2
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1
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5.1k
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Answer: Answer: Mapping fastq files with paired reads and member of the paired reads not present
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
0
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1
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6.7k
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Comment: Comment: Sequence extraction from a fastq file
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
2
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0
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6.7k
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Answer: Answer: Sequence extraction from a fastq file
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
0
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0
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13k
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Comment: Comment: gtf file for htseq count
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
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2.4k
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Comment: Comment: Variation Statistics on bam file over all reads
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
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0
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2.4k
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Comment: C: Extract sequences from genome
11.0 years ago by Ashutosh Pandey 12k
0
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1
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4.0k
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Answer: A: How to anntate small-RNA seq reads distribution
11.0 years ago by Ashutosh Pandey 12k
0
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0
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7.6k
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Comment: C: Extracting paired-end reads on different contigs from bam file
11.0 years ago by Ashutosh Pandey 12k
2
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0
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7.6k
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Answer: Answer: Extracting paired-end reads on different contigs from bam file
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
1
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1
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4.2k
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Answer: Answer: Need some help regarding format compatible with VEP online tools
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
0
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0
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3.4k
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Comment: Comment: N as ALT allele
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
1
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0
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1.7k
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Comment: Comment: developing biopython - a tool which doesn't exist but could be usful
updated 3.8 years ago by 45k • written 11.0 years ago by 12k
2
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1
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21k
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Comment: Comment: how to use log transformation with read count data?
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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1
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3.4k
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Comment: Comment: N as ALT allele
updated 4.0 years ago by 45k • written 11.1 years ago by 12k
0
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1
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3.4k
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Comment: C: N as ALT allele
11.1 years ago by Ashutosh Pandey 12k
0
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0
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4.1k
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Answer: Answer: How to estimate batch effect in microarray gene expression data?
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
1
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1
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2.7k
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Comment: Comment: where are parameters of SNPQ(snp quality) and TD(total read depth) defined when
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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1
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4.1k
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Comment: Comment: how to export RNA-seq reads which mapped to genes?
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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1
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4.1k
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Comment: Comment: how to export RNA-seq reads which mapped to genes?
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
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0
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4.1k
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Comment: Comment: Tophat2 Library Type Choice
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
1
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2
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4.1k
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Comment: Comment: Tophat2 Library Type Choice
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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0
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3.9k
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Comment: Comment: how to filter at the information of DP(read depth at this position for this samp
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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0
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4.9k
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Comment: Comment: Difference between Gene Models (Annotation files .gtf) for human (hg19)
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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1
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4.9k
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Comment: Comment: Difference between Gene Models (Annotation files .gtf) for human (hg19)
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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1
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5.6k
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Comment: Comment: How do we distinguish between SNP/INDEL/SV in 1000 genomes Phase 3 data
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
0
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1
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4.1k
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Comment: Comment: Alignment Tools for Gene Coexpression Networks
updated 3.8 years ago by 45k • written 11.1 years ago by 12k
3
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0
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4.3k
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Answer: Answer: SNP calling from pooled RNA-seq data
updated 4.6 years ago by 45k • written 11.1 years ago by 12k
1,162 results • Page 9 of 24
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