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Comment: C: Is there any C API documentation for HTSLIB?
7.6 years ago by chen ★ 2.5k
5
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8
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5.7k
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Is there any C API documentation for HTSLIB?
htslib API Doc BAM
updated 7.6 years ago by 104k • written 7.6 years ago by ★ 2.5k
1
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1
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5.5k
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Comment: C: Multiple Hist and Unique Mapped Reads
7.6 years ago by chen ★ 2.5k
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0
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4.7k
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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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0
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9.4k
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Comment: C: How to decompress several fastq.gz files into one single file?
7.6 years ago by chen ★ 2.5k
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2
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9.4k
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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
0
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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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0
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5.9k
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Comment: C: Python: extract barcodes and vector sequence from fastq reads, add barcodes to h
7.6 years ago by chen ★ 2.5k
1
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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
0
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0
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3.6k
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Answer: A: sra to fastq
7.6 years ago by chen ★ 2.5k
0
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0
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3.6k
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Comment: C: sra to fastq
7.6 years ago by chen ★ 2.5k
0
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1
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6.9k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
1
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0
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6.9k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
0
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1
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1.9k
views
Comment: C: Detection of CNVs
7.6 years ago by chen ★ 2.5k
0
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0
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1.9k
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Comment: C: Detection of CNVs
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
0
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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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5.9k
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Answer: A: How to make new VCF files myself?
7.6 years ago by chen ★ 2.5k
0
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0
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6.9k
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Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
0
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0
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6.9k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
0
votes
0
replies
6.9k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
1
vote
0
replies
6.9k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
0
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0
replies
6.9k
views
Comment: C: MutScan: Detect important mutations by scanning FastQ files directly
7.6 years ago by chen ★ 2.5k
0
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1
reply
6.9k
views
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
views
Answer: A: Sudden quality drop in the middle of HiSeq R1 reads but not in R2?
7.8 years ago by chen ★ 2.5k
9
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7
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6.8k
views
6 follow
How to detect CNV with panel sequencing?
CNV panel sequencing capturing control
updated 7.8 years ago by • 0 • written 8.2 years ago by ★ 2.5k
0
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1
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4.7k
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Answer: A: Paired-end reads: Sequence length is different between read 1 and 2
7.9 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
1
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0
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3.0k
views
Comment: C: concatenate using cat
7.9 years ago by chen ★ 2.5k
0
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1
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3.0k
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Answer: A: concatenate using cat
7.9 years ago by chen ★ 2.5k
0
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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
0
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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
views
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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3.6k
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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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3.6k
views
Answer: A: How to get per sample read depth from VCF with no DP field
7.9 years ago by chen ★ 2.5k
0
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0
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1.4k
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Answer: A: merging PE reads in Single cell transcriptome
8.0 years ago by chen ★ 2.5k
0
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0
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3.0k
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Answer: A: Biopython - calculate overlap between two sequences
8.0 years ago by chen ★ 2.5k
0
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0
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18k
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Comment: C: Fastq Files From Different Flowcells
8.0 years ago by chen ★ 2.5k
0
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2
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1.3k
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Are there big DNA difference of HPV 16/18/31/32 and other HPVs?
HPV
updated 8.0 years ago by ▴ 870 • written 8.0 years ago by ★ 2.5k
6
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0
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9.8k
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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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0
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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
2
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0
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8.2k
views
Comment: C: AfterQC: Automatic Filtering, Trimming, Error Removing and Quality Control for f
8.0 years ago by chen ★ 2.5k
0
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0
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4.2k
views
Answer: A: overlapping nucleotides in sequence alignment
8.0 years ago by chen ★ 2.5k
0
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1
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1.7k
views
Answer: A: how to detect repetitive motifs in gene?
8.0 years ago by chen ★ 2.5k
0
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0
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8.4k
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Answer: A: Should I work first in a Bioinformatics company or get a Ph. D.?
8.1 years ago by chen ★ 2.5k
0
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0
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4.0k
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Answer: A: Remove duplicates from exome sequencing data
8.1 years ago by chen ★ 2.5k
0
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0
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6.7k
views
Comment: A: Download all DNA mutations from TCGA
8.1 years ago by chen ★ 2.5k
4
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1
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1.6k
views
Answer: A: How to add read depth to gene of my interest
8.1 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
8.1 years ago by chen ★ 2.5k
0
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1
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3.7k
views
Answer: A: Java or C++ (which side should I choose)
8.1 years ago by chen ★ 2.5k
218 results • Page 4 of 5
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