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Comment: C: MutScan: detect and visualize target mutations by just scanning FastQ, 50X faste
8.5 years ago by chen ★ 2.5k
1
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1
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2.9k
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Answer: A: Where can I find NGS data to test alignment and SNP detection tool
8.8 years ago by chen ★ 2.5k
16
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8
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2.9k
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8 follow
Forum: What are the most important unresolved problems in Bioinformatics?
bioinformatics
updated 2.2 years ago by 45k • written 9.0 years ago by ★ 2.5k
1
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1
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5.4k
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Answer: A: Establishing a Bioinformatics Core Facilities
8.9 years ago by chen ★ 2.5k
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2.0k
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Comment: C: Most accurate way to measure adapters quantity in NGS illumina reads
8.9 years ago by chen ★ 2.5k
1
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1
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2.0k
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Answer: A: Most accurate way to measure adapters quantity in NGS illumina reads
8.9 years ago by chen ★ 2.5k
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6.6k
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Comment: C: Is there any C API documentation for HTSLIB?
8.9 years ago by chen ★ 2.5k
0
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1
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6.6k
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Comment: C: Is there any C API documentation for HTSLIB?
8.9 years ago by chen ★ 2.5k
5
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8
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6.6k
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Is there any C API documentation for HTSLIB?
htslib API Doc BAM
updated 8.9 years ago by 105k • written 8.9 years ago by ★ 2.5k
1
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1
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6.5k
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Comment: C: Multiple Hist and Unique Mapped Reads
8.9 years ago by chen ★ 2.5k
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5.7k
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Answer: A: Is microarray gene expression analysis is dead ?
8.9 years ago by chen ★ 2.5k
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0
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11k
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Comment: C: How to decompress several fastq.gz files into one single file?
9.0 years ago by chen ★ 2.5k
1
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2
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11k
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Answer: A: How to decompress several fastq.gz files into one single file?
9.0 years ago by chen ★ 2.5k
0
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0
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23k
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Answer: A: NGS BWA Installing
9.0 years ago by chen ★ 2.5k
0
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0
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6.5k
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Comment: C: Python: extract barcodes and vector sequence from fastq reads, add barcodes to h
9.0 years ago by chen ★ 2.5k
1
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1
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6.5k
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Answer: A: Python: extract barcodes and vector sequence from fastq reads, add barcodes to h
9.0 years ago by chen ★ 2.5k
0
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0
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4.7k
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Answer: A: sra to fastq
9.0 years ago by chen ★ 2.5k
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0
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4.7k
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Comment: C: sra to fastq
9.0 years ago by chen ★ 2.5k
0
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1
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8.5k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
1
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0
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8.5k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
0
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1
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2.4k
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Comment: C: Detection of CNVs
9.0 years ago by chen ★ 2.5k
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0
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2.4k
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Comment: C: Detection of CNVs
9.0 years ago by chen ★ 2.5k
2
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20k
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Answer: A: What is a bam.bai for?
9.0 years ago by chen ★ 2.5k
0
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2
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2.4k
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Answer: A: Detection of CNVs
9.0 years ago by chen ★ 2.5k
1
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0
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6.9k
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Answer: A: How to make new VCF files myself?
9.0 years ago by chen ★ 2.5k
0
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0
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8.5k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
0
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0
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8.5k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
0
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0
replies
8.5k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
1
vote
0
replies
8.5k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
0
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0
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8.5k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
0
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1
reply
8.5k
views
Answer: A: MutScan: Detect important mutations by scanning FastQ files directly
9.0 years ago by chen ★ 2.5k
4
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2
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7.6k
views
Answer: A: Sudden quality drop in the middle of HiSeq R1 reads but not in R2?
9.1 years ago by chen ★ 2.5k
9
votes
7
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7.6k
views
6 follow
How to detect CNV with panel sequencing?
CNV panel sequencing capturing control
updated 9.1 years ago by • 0 • written 9.5 years ago by ★ 2.5k
0
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1
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5.3k
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Answer: A: Paired-end reads: Sequence length is different between read 1 and 2
9.2 years ago by chen ★ 2.5k
1
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0
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2.3k
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Answer: A: Node requirement on a cluster for bioinformatics analysis
9.2 years ago by chen ★ 2.5k
1
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0
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3.9k
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Comment: C: concatenate using cat
9.2 years ago by chen ★ 2.5k
0
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1
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3.9k
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Answer: A: concatenate using cat
9.2 years ago by chen ★ 2.5k
0
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0
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1.7k
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Answer: A: Frequency of codon mutation in cancer
9.2 years ago by chen ★ 2.5k
0
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0
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11k
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Answer: A: Ucsc Gene Name Question
9.2 years ago by chen ★ 2.5k
1
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1
reply
7.0k
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Answer: A: Trim & align paired-end reads in a single pass
9.2 years ago by chen ★ 2.5k
0
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1
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4.1k
views
Answer: A: How to get per sample read depth from VCF with no DP field
9.3 years ago by chen ★ 2.5k
1
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1
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4.1k
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Answer: A: How to get per sample read depth from VCF with no DP field
9.3 years ago by chen ★ 2.5k
0
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0
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1.7k
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Answer: A: merging PE reads in Single cell transcriptome
9.3 years ago by chen ★ 2.5k
0
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0
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3.3k
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Answer: A: Biopython - calculate overlap between two sequences
9.3 years ago by chen ★ 2.5k
0
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0
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20k
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Comment: C: Fastq Files From Different Flowcells
9.3 years ago by chen ★ 2.5k
0
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2
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1.6k
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Are there big DNA difference of HPV 16/18/31/32 and other HPVs?
HPV
updated 9.4 years ago by ▴ 870 • written 9.4 years ago by ★ 2.5k
6
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0
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13k
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Answer: A: Good Habit for Bioinformatics Analyst or Scientist
updated 9.4 years ago by 27k • written 9.4 years ago by ★ 2.5k
2
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0
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2.3k
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Answer: A: How to choose a variant filtering criteria to reduce false positives
9.4 years ago by chen ★ 2.5k
2
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0
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9.4k
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Comment: C: AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for f
9.4 years ago by chen ★ 2.5k
0
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0
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4.7k
views
Answer: A: overlapping nucleotides in sequence alignment
9.4 years ago by chen ★ 2.5k
225 results • Page 4 of 5
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