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Answer: A: Tool For Counting Adapter Dimer: I need metrics NOT trimming
6.7 years ago by chen ★ 2.5k
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8.2k
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Answer: A: AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for f
6.8 years ago by chen ★ 2.5k
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2
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1.3k
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Answer: A: Assembly of two ends of the sequence
7.0 years ago by chen ★ 2.5k
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3.3k
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Answer: C: Is there a consensus that Matlab is the wrong language for open-access bioinform
7.1 years ago by chen ★ 2.5k
1
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1
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2.3k
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Answer: A: Where can I find NGS data to test alignment and SNP detection tool
7.4 years ago by chen ★ 2.5k
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3.9k
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Answer: A: Establishing a Bioinformatics Core Facilities
7.5 years ago by chen ★ 2.5k
1
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1
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1.6k
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Answer: A: Most accurate way to measure adapters quantity in NGS illumina reads
7.5 years ago by chen ★ 2.5k
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4.6k
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Answer: A: Is microarray gene expression analysis is dead ?
7.6 years ago by chen ★ 2.5k
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2
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9.3k
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Answer: A: How to decompress several fastq.gz files into one single file?
7.6 years ago by chen ★ 2.5k
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0
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21k
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Answer: A: NGS BWA Installing
7.6 years ago by chen ★ 2.5k
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1
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5.9k
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Answer: A: Python: extract barcodes and vector sequence from fastq reads, add barcodes to h
7.6 years ago by chen ★ 2.5k
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3.5k
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Answer: A: sra to fastq
7.6 years ago by chen ★ 2.5k
2
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0
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17k
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Answer: A: What is a bam.bai for?
7.6 years ago by chen ★ 2.5k
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2
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1.9k
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Answer: A: Detection of CNVs
7.6 years ago by chen ★ 2.5k
1
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0
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5.8k
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Answer: A: How to make new VCF files myself?
7.6 years ago by chen ★ 2.5k
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1
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6.9k
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Answer: A: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
4
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2
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6.0k
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Answer: A: Sudden quality drop in the middle of HiSeq R1 reads but not in R2?
7.7 years ago by chen ★ 2.5k
0
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1
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4.6k
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Answer: A: Paired-end reads: Sequence length is different between read 1 and 2
7.8 years ago by chen ★ 2.5k
1
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0
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1.7k
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Answer: A: Node requirement on a cluster for bioinformatics analysis
7.9 years ago by chen ★ 2.5k
0
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1
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2.9k
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Answer: A: concatenate using cat
7.9 years ago by chen ★ 2.5k
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0
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1.4k
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Answer: A: Frequency of codon mutation in cancer
7.9 years ago by chen ★ 2.5k
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0
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10k
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Answer: A: Ucsc Gene Name Question
7.9 years ago by chen ★ 2.5k
1
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1
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6.0k
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Answer: A: Trim & align paired-end reads in a single pass
7.9 years ago by chen ★ 2.5k
0
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1
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3.5k
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Answer: A: How to get per sample read depth from VCF with no DP field
7.9 years ago by chen ★ 2.5k
1
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1
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3.5k
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Answer: A: How to get per sample read depth from VCF with no DP field
7.9 years ago by chen ★ 2.5k
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0
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1.4k
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Answer: A: merging PE reads in Single cell transcriptome
7.9 years ago by chen ★ 2.5k
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0
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3.0k
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Answer: A: Biopython - calculate overlap between two sequences
7.9 years ago by chen ★ 2.5k
6
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0
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9.7k
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Answer: A: Good Habit for Bioinformatics Analyst or Scientist
updated 8.0 years ago by 26k • written 8.0 years ago by ★ 2.5k
2
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2.1k
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Answer: A: How to choose a variant filtering criteria to reduce false positives
8.0 years ago by chen ★ 2.5k
0
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0
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4.1k
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Answer: A: overlapping nucleotides in sequence alignment
8.0 years ago by chen ★ 2.5k
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1
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1.7k
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Answer: A: how to detect repetitive motifs in gene?
8.0 years ago by chen ★ 2.5k
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0
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8.3k
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Answer: A: Should I work first in a Bioinformatics company or get a Ph. D.?
8.0 years ago by chen ★ 2.5k
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0
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3.9k
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Answer: A: Remove duplicates from exome sequencing data
8.0 years ago by chen ★ 2.5k
4
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1
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1.6k
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Answer: A: How to add read depth to gene of my interest
8.0 years ago by chen ★ 2.5k
0
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0
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16k
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Answer: A: fasta - reverse complement sequence
8.0 years ago by chen ★ 2.5k
0
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1
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3.7k
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Answer: A: Java or C++ (which side should I choose)
8.0 years ago by chen ★ 2.5k
1
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1
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32k
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Answer: A: How To Organize A Pipeline Of Small Scripts Together?
8.0 years ago by chen ★ 2.5k
2
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0
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1.9k
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Answer: A: How to build Biostar?
8.0 years ago by chen ★ 2.5k
2
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0
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16k
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Answer: A: Annotating bed file with gene names
8.0 years ago by chen ★ 2.5k
3
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1
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19k
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Answer: A: pybam - 100% python BAM reader
8.0 years ago by chen ★ 2.5k
1
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0
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5.0k
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Answer: A: Reads Simulation and Read Simulator
8.1 years ago by chen ★ 2.5k
0
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0
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2.0k
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Answer: A: Which software to use to map 100bp DNA sequence to genome
8.1 years ago by chen ★ 2.5k
2
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2
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3.1k
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Answer: A: How to change the quality score of reads ? (quick help is appreciated)
8.1 years ago by chen ★ 2.5k
2
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1
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2.7k
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Answer: A: Fix FoxG1 deletion in my son using CRISPR
8.1 years ago by chen ★ 2.5k
1
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0
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6.7k
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Answer: A: Interpretation of FASTQC results - do I need to trim my sequence?
8.1 years ago by chen ★ 2.5k
2
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1
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3.0k
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Answer: A: Simulate Ngs Reads With Exact Mutations (Snp, Indel Etc.) , Frequency , Forward
8.1 years ago by chen ★ 2.5k
0
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0
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2.0k
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Answer: A: About possible bias due to different experimental design
8.1 years ago by chen ★ 2.5k
1
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1
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2.4k
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Answer: A: Sort specific reads from fastq
8.1 years ago by chen ★ 2.5k
1
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0
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11k
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Answer: A: Why GATK and bcftools SNP calling different?
8.1 years ago by chen ★ 2.5k
1
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0
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12k
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Answer: Answer: How to remove poly T in RNA-sequencing data
updated 16 months ago by 43k • written 8.7 years ago by ★ 2.5k
100 results • Page 2 of 2
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