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5.9k
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Answer: A: IGV for RNA-SEQ
updated 3.0 years ago by 37k • written 8.6 years ago by 7.4k
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1
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3.0k
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Answer: A: Picardtools Output of CollectRNAMetrices
updated 3.0 years ago by 37k • written 7.0 years ago by 7.4k
5
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0
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2.4k
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Answer: A: Genetics and the Origin of Species
updated 3.0 years ago by 37k • written 8.6 years ago by 7.4k
0
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1
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8.0k
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Answer: A: difference between BWA mem, sampe and bwasw
updated 3.1 years ago by 37k • written 7.0 years ago by 7.4k
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0
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2.7k
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Answer: A: Bed file score , mismatch , and other column information
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
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1
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3.8k
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Answer: Answer: Retrieve the FASTA transcript sequences of a list of NCBI genes
updated 9 months ago by 37k • written 7.8 years ago by 7.4k
5
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1
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11k
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Answer: A: What is the best programming language for NGS data analysis pipeline development
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
2
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2
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4.0k
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Answer: A: Fast search for many patterns
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
2
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1
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2.9k
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Answer: A: BWA index segmentation fault for specific sequence
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
4
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0
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11k
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Answer: A: What is the best programming language for NGS data analysis pipeline development
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
2
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1
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3.7k
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Answer: A: reheadering, merging and sorting on different bam file
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
3
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1
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3.5k
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Answer: A: Download all hg19 coding sequences from UCSC
updated 3.1 years ago by 37k • written 8.7 years ago by 7.4k
2
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1
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3.1k
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Answer: A: Add a seq (the outgroup) to the top of its corresponding gene
updated 3.1 years ago by 37k • written 8.8 years ago by 7.4k
3
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0
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3.0k
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Answer: A: BWA and SOAP2 cannot map a particular sequence which exists in the genome
updated 3.1 years ago by 37k • written 8.8 years ago by 7.4k
4
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3
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3.3k
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Answer: A: Bioinformatics vs. the Climate Crisis
3.2 years ago by Dan D 7.4k
1
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1
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2.4k
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Answer: A: CONTRA ERRORS (need urgent help!!!)
updated 3.2 years ago by 37k • written 7.5 years ago by 7.4k
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0
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3.6k
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Answer: A: Splitting paired end bam files
updated 3.2 years ago by 37k • written 7.6 years ago by 7.4k
7
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1
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2.1k
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Answer: A: Bioinformatician, a jack of all trades, but in the eye of the CV-beholder a mast
3.3 years ago by Dan D 7.4k
0
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3
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3.8k
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Answer: Answer: Freebayes and snpeff give different number of SNPs
updated 10 months ago by 37k • written 8.1 years ago by 7.4k
0
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1
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4.5k
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Answer: Answer: Counting number of bases covered across multiple bam files
updated 11 months ago by 37k • written 8.2 years ago by 7.4k
3
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0
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4.1k
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Answer: A: markDuplicates: Histogram not produced
updated 3.3 years ago by 37k • written 8.3 years ago by 7.4k
6
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1
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5.4k
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Answer: A: tophat- paired end reads combined in one file
updated 3.3 years ago by 37k • written 8.4 years ago by 7.4k
3
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1
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5.4k
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Answer: A: FastQC and EstimateLibrarySize (Picard): Library Complexity and/or Duplicated Re
updated 3.3 years ago by 37k • written 8.6 years ago by 7.4k
2
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0
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3.8k
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Answer: A: How can I get the informaiton about base quality(BQ) in VCF file?
updated 3.3 years ago by 37k • written 8.8 years ago by 7.4k
3
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1
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6.8k
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Answer: A: Bwa or bowtie for mapping mulitple genomes
updated 3.3 years ago by 37k • written 8.8 years ago by 7.4k
15
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1
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23k
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Answer: A: Human dna reference file with no prefix 'chr'
updated 3.3 years ago by 37k • written 8.2 years ago by 7.4k
1
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1
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2.6k
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Answer: A: interval_list for hg38
3.4 years ago by Dan D 7.4k
0
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0
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2.3k
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Answer: C: Does anyone know how the Y axis (% of reference) for the "coverage distribution"
updated 3.6 years ago by 37k • written 8.6 years ago by 7.4k
0
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2
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3.7k
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Answer: A: How to interpret reference homozygous genotype in the VCF file generated by GATK
updated 3.6 years ago by 37k • written 8.4 years ago by 7.4k
1
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0
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5.1k
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Answer: A: Demultiplexing bcl files into fastq files
updated 3.7 years ago by 37k • written 5.4 years ago by 7.4k
4
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1
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4.1k
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Answer: A: Get Random Alignments From Sam File
updated 4.0 years ago by 37k • written 9.4 years ago by 7.4k
0
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1
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14k
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Answer: A: Demultiplexing fastq files with dual barcodes
updated 4.1 years ago by 37k • written 7.8 years ago by 7.4k
2
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0
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2.1k
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Answer: A: Notable open source bioinformatics projects written in Java?
updated 4.4 years ago by 37k • written 6.9 years ago by 7.4k
21
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1
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28k
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Answer: A: I loaded a BAM (RNA-seq) file into IGV but cant see anything!
updated 4.4 years ago by 37k • written 8.2 years ago by 7.4k
0
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1
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1.6k
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Answer: A: Visualization of chromosomal locations
updated 4.4 years ago by 37k • written 6.9 years ago by 7.4k
2
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1
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1.2k
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Answer: A: Hetero and Euchromatin
updated 4.4 years ago by 37k • written 6.9 years ago by 7.4k
2
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0
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2.1k
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Answer: A: Rat rn5 GTF format
updated 4.4 years ago by 37k • written 6.9 years ago by 7.4k
0
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0
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8.4k
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Answer: A: Project Euler Equivalent For Bioinformatics?
updated 4.4 years ago by 37k • written 8.8 years ago by 7.4k
1
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0
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3.0k
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Answer: A: using bash variable in picard MarkDuplicates command
4.5 years ago by Dan D 7.4k
1
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1
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2.6k
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Answer: A: Removing Indices using Cutadapt
4.7 years ago by Dan D 7.4k
1
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0
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1.5k
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Answer: A: How does picard CollectWGSmetrics estimate coverage on Soft-Clipped Reads?
5.0 years ago by Dan D 7.4k
1
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0
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3.8k
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Answer: C: Faster reading sequences from a fastq file
5.0 years ago by Dan D 7.4k
1
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0
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4.3k
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Answer: A: Newbie question: how to create BWA index from multiple .fasta files
5.1 years ago by Dan D 7.4k
1
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1
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3.4k
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Answer: A: Picard alignment statistics error
5.3 years ago by Dan D 7.4k
1
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0
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3.2k
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Answer: A: How to upload fasta file to SSH Supercomputer
5.4 years ago by Dan D 7.4k
0
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1
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7.6k
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Answer: A: How to split a fastq file into each corresponding sample.fastq?
5.4 years ago by Dan D 7.4k
2
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1
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1.9k
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Answer: A: Is it possible to get VCF from two fastq files without reference genome?
5.4 years ago by Dan D 7.4k
0
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1
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3.8k
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Answer: A: Strand colour from BED file in IGV
5.4 years ago by Dan D 7.4k
2
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1
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1.8k
views
Answer: A: Custom features in IGV
5.4 years ago by Dan D 7.4k
1
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1
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1.2k
views
Answer: A: Is there any software that can highlight or show the paired end reads within .sa
5.5 years ago by Dan D 7.4k
201 results • Page 1 of 5
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