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Comment: Comment: Query related to MIseq, NextSeq illumina platform
updated 3.4 years ago by 45k • written 10.6 years ago by 13k
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Answer: Answer: trouble with Install eXpress
updated 3.4 years ago by 45k • written 10.6 years ago by 13k
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Comment: Comment: Validated CNV dataset for NA12878
updated 3.7 years ago by 45k • written 10.6 years ago by 13k
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4.3k
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Comment: C: SimPlot on Mac OS
10.6 years ago by User 59 13k
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3.8k
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Comment: Comment: How to set up and run Mugsy software on Linux 11.04?
updated 3.5 years ago by 45k • written 10.6 years ago by 13k
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3.8k
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Answer: Answer: How to set up and run Mugsy software on Linux 11.04?
updated 3.5 years ago by 45k • written 10.6 years ago by 13k
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3.4k
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Comment: Comment: Ideal coverage required for PacBio error correction using HGAP
updated 3.5 years ago by 45k • written 10.7 years ago by 13k
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2.0k
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Job: Two Customer Liaison Officer positions open in the Platforms & Pipelines Group at TGAC
tgac genomics sequencing ngs
updated 3.5 years ago by 45k • written 10.7 years ago by 13k
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Comment: Comment: BWA vs Bowtie 2 (Poll)
updated 3.5 years ago by 45k • written 10.7 years ago by 13k
7
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43k
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Comment: Comment: BWA vs Bowtie 2 (Poll)
updated 3.5 years ago by 45k • written 10.7 years ago by 13k
4
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10k
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Comment: Comment: Notepad and word will not read Fastq or FASTA files
updated 3.5 years ago by 45k • written 10.7 years ago by 13k
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5.3k
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Comment: Comment: Contamination Check using HET/HOM
updated 3.6 years ago by 45k • written 10.7 years ago by 13k
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5.3k
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Comment: Comment: Contamination Check using HET/HOM
updated 3.6 years ago by 45k • written 10.7 years ago by 13k
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1
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2.9k
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Comment: Comment: replacing 'N' with 'A', 'C', 'G', or 'T' from ABI file (sanger)
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
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2
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Answer: Answer: abyss-fac: command not found on Kubuntu 14.04
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
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Answer: Answer: Human Exome GC content
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
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8.4k
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Comment: Comment: Bioinformatics commercial services as a risk factor for scientific misconduct
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
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8.4k
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Comment: Comment: Bioinformatics commercial services as a risk factor for scientific misconduct
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
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2.1k
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Answer: Answer: The FGT test
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
2
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2.4k
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Answer: Answer: NGSrich target enrichment: software error
updated 3.6 years ago by 45k • written 10.8 years ago by 13k
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1
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8.7k
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Comment: Comment: Validated CNV dataset for NA12878
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
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5.2k
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Answer: Answer: Illumina sequence identifiers conversion
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
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1
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3.3k
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Answer: Answer: Basic Course/Training on Developing Tools
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
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4.5k
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Comment: Comment: What causes this message in IGV?
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
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5.9k
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Comment: C: Freebayes and snpeff give different number of SNPs
10.9 years ago by User 59 13k
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5.9k
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Comment: C: Freebayes and snpeff give different number of SNPs
10.9 years ago by User 59 13k
1
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3.0k
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Answer: Answer: DNA-seq PE150 BWA alignment
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
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1
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4.5k
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Answer: Answer: What causes this message in IGV?
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
2
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2.6k
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Answer: Answer: Micro RNA docking
updated 3.7 years ago by 45k • written 10.9 years ago by 13k
1
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0
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8.4k
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Comment: C: ClinVar download sources
11.1 years ago by User 59 13k
2
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7.6k
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Comment: Comment: Best Variation Analysis Software which can support VCF file Format?
updated 4.6 years ago by 45k • written 11.1 years ago by 13k
2
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1
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22k
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Answer: A: Why is Hadoop not used a lot in bio-informatics?
11.1 years ago by User 59 13k
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1
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4.2k
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Comment: C: Does read-depth refer to a fold?
11.1 years ago by User 59 13k
2
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5.8k
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Comment: C: Open Source Diploid Variant Caller comparable to GATK Haplotype Caller?
11.1 years ago by User 59 13k
1
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3.5k
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Comment: Comment: Human Whole blood transcriptome 10 or 30 Million reads
updated 3.8 years ago by 45k • written 11.1 years ago by 13k
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5.8k
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Comment: Comment: Open Source Compliant Diploid Variant Caller comparable to GATK Haplotype Caller
updated 3.8 years ago by 45k • written 11.1 years ago by 13k
6
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1
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5.8k
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Answer: Answer: Open Source Compliant Diploid Variant Caller comparable to GATK Haplotype Caller
updated 3.8 years ago by 45k • written 11.1 years ago by 13k
0
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1
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3.5k
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Comment: C: Human Whole blood transcriptome 10 or 30 Million reads
11.1 years ago by User 59 13k
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0
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3.4k
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Comment: Comment: Quality of whole genome sequencing and whole exome sequencing
updated 3.8 years ago by 45k • written 11.1 years ago by 13k
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13k
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Comment: C: how to identify a sequencing sample's gender
11.2 years ago by User 59 13k
1
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0
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9.8k
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Comment: C: Curious about gene fusion in exome seuquencing data.
11.2 years ago by User 59 13k
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1
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9.8k
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Comment: C: Curious about gene fusion in exome seuquencing data.
11.2 years ago by User 59 13k
1
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1
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2.9k
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Answer: Answer: dbSNP b126 in vcf format
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
2
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1
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2.7k
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Answer: Answer: which one would be the better way for RNA-seq Experiment design
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
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3.5k
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Comment: Comment: bfast index is so hard
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
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4.2k
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Comment: Comment: gene (or SNP) related to a disease
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
3
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6.2k
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Answer: A: Haloplex & Allele Calling
11.2 years ago by User 59 13k
0
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1
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2.7k
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Comment: Comment: Problems compiling the Bam_readcount program
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
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4.7k
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Comment: Comment: Bioinformatician vs. wet-lab scientist saleries in industry
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
8
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7.7k
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Answer: Answer: What happened with miRecords mirna database website ?
updated 3.9 years ago by 45k • written 11.2 years ago by 13k
658 results • Page 5 of 14
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