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Comment: C: Large VCF QUAL Values
8.8 years ago by Zaag ▴ 870
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Answer: A: Large VCF QUAL Values
8.8 years ago by Zaag ▴ 870
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Comment: C: 3-year Joint PhD studentship with the University of Birmingham and Maastricht Un
8.8 years ago by Zaag ▴ 870
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7.3k
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Answer: A: Does anyone use Python for variant calling?
8.8 years ago by Zaag ▴ 870
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3.4k
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Answer: A: What is best commercial software for exome/genome interpretation?
8.8 years ago by Zaag ▴ 870
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5.9k
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Comment: C: GATK GenotypeGVCFs 8 weeks runtime
9.0 years ago by Zaag ▴ 870
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5.9k
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Comment: C: GATK GenotypeGVCFs 8 weeks runtime
9.0 years ago by Zaag ▴ 870
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3.0k
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Comment: C: RRBS and Ilumina read size
9.0 years ago by Zaag ▴ 870
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11k
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Comment: C: [Python] How to convert a list to a dictionary if dict() does not work without u
9.0 years ago by Zaag ▴ 870
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1
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11k
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Answer: A: [Python] How to convert a list to a dictionary if dict() does not work without u
9.0 years ago by Zaag ▴ 870
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12k
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Comment: C: bwa mem seq and Segmentation fault (core dumped)
9.0 years ago by Zaag ▴ 870
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1
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12k
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Comment: C: bwa mem seq and Segmentation fault (core dumped)
9.0 years ago by Zaag ▴ 870
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12k
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Comment: C: bwa mem seq and Segmentation fault (core dumped)
9.0 years ago by Zaag ▴ 870
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4.3k
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Comment: C: vcf files in gatk not showing data lines
9.0 years ago by Zaag ▴ 870
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2
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2.2k
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Answer: A: Python or shell scripting code ro count individual mapped reads of amplicons
9.0 years ago by Zaag ▴ 870
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2.4k
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Answer: A: Variant annotation tool
9.0 years ago by Zaag ▴ 870
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1
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6.0k
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Comment: C: Targeted NGS: amplicon length vs read length
9.0 years ago by Zaag ▴ 870
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1
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6.0k
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Comment: C: Targeted NGS: amplicon length vs read length
9.0 years ago by Zaag ▴ 870
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1.9k
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Comment: C: Can anyone suggest some good research papers to understand the complete NGS work
9.1 years ago by Zaag ▴ 870
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3.1k
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Answer: A: Perl help regarding hash
9.1 years ago by Zaag ▴ 870
2
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80k
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Comment: C: How Much Coverage Do We Need For An Rna-Seq Experiment?
9.2 years ago by Zaag ▴ 870
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2.3k
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Answer: A: Nextseq 500 sample exome data
9.2 years ago by Zaag ▴ 870
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1
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11k
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Comment: C: Snptest (Gen/Sample) Files To R
9.2 years ago by Zaag ▴ 870
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4.1k
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Comment: C: Peak calling with MACS for DNase-seq data and Peak annotation by Homer
9.3 years ago by Zaag ▴ 870
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7.1k
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Answer: A: Fisher Strand in GATK, a good measure to detect Strand Bias?
9.4 years ago by Zaag ▴ 870
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25k
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Comment: Comment: How To Use Coordinates In Order To Extract Sequences In Fasta File?
updated 2.6 years ago by 45k • written 9.5 years ago by ▴ 870
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1
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3.3k
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Comment: C: How to remove primers from a Roche 454 sff file
9.6 years ago by Zaag ▴ 870
1
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0
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5.3k
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Answer: Answer: Showing both strands in IGV, or if not possible what genome viewer is good for s
updated 2.6 years ago by 45k • written 9.6 years ago by ▴ 870
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3.8k
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Comment: C: extract data from txt files
9.6 years ago by Zaag ▴ 870
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0
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4.9k
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Answer: Answer: variant calling on amplicon data
updated 2.5 years ago by 45k • written 9.6 years ago by ▴ 870
3
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1
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4.9k
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Comment: Comment: variant calling on amplicon data
updated 2.5 years ago by 45k • written 9.6 years ago by ▴ 870
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1
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2.2k
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Comment: Comment: When I use XHMM to analyze CNV,I found this error,do not know how to adjust?
updated 2.5 years ago by 45k • written 9.6 years ago by ▴ 870
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10k
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Comment: C: Bait/Target files for Picard HsMetrics (Exome Sequencing)
9.6 years ago by Zaag ▴ 870
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1
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10k
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Comment: C: Bait/Target files for Picard HsMetrics (Exome Sequencing)
9.6 years ago by Zaag ▴ 870
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0
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10k
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Comment: Comment: Bait/Target files for Picard HsMetrics (Exome Sequencing)
updated 2.5 years ago by 45k • written 9.6 years ago by ▴ 870
0
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1
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10k
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Answer: Answer: Bait/Target files for Picard HsMetrics (Exome Sequencing)
updated 2.5 years ago by 45k • written 9.6 years ago by ▴ 870
2
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4.9k
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Answer: Answer: GATK IndelRealigner issue "TOO MANY READS"
updated 2.3 years ago by 45k • written 9.8 years ago by ▴ 870
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1
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14k
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Comment: C: Convert BED(UCSC) to VCF
9.8 years ago by Zaag ▴ 870
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8.0k
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Comment: C: How can you convert a GATK interval_list file into a BED file
9.8 years ago by Zaag ▴ 870
2
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2.2k
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Answer: A: Good tool for viewing Multiallelic vcf/bcf files
9.8 years ago by Zaag ▴ 870
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3.3k
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Comment: C: BWA vs Bowtie2 output
9.8 years ago by Zaag ▴ 870
4
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1
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3.5k
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Answer: Answer: Whole Genome Sequence (WGS) throughput (FastQC, Picard)
updated 2.2 years ago by 45k • written 9.8 years ago by ▴ 870
2
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0
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3.8k
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Answer: Answer: Questions regarding proprocess for raw data and usage of FastQC
updated 2.2 years ago by 45k • written 9.9 years ago by ▴ 870
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1.5k
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Answer: Answer: Exome Sequencing Resources
updated 3.9 years ago by 45k • written 9.9 years ago by ▴ 870
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4.3k
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Comment: Comment: Alternatives to LifeScope for realigning SOLiD BAM files
updated 2.7 years ago by 45k • written 10.0 years ago by ▴ 870
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0
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4.3k
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Answer: Answer: Alternatives to LifeScope for realigning SOLiD BAM files
updated 2.8 years ago by 45k • written 10.0 years ago by ▴ 870
0
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2.6k
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Comment: Comment: Default sequencing keys and flow order
updated 2.8 years ago by 45k • written 10.0 years ago by ▴ 870
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0
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2.8k
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Comment: Comment: Is there software that takes advantage of MarkedDuplicates for SNP calling?
updated 2.8 years ago by 45k • written 10.0 years ago by ▴ 870
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2.9k
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Answer: A: Variant Analysis on MiSeq Data
10.0 years ago by Zaag ▴ 870
0
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0
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11k
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Comment: C: BWA alignment using paired end reads from different lanes
10.0 years ago by Zaag ▴ 870
102 results • Page 2 of 3
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