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Comment: C: Method for analyzing Targeted re-sequencing based on Ligation Mediated PCR?
updated 5.8 years ago by 45k • written 9.8 years ago by ▴ 870
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Answer: Answer: What is your preferred annotation techniques when you analyze mutation in exome
updated 2.8 years ago by 45k • written 10.4 years ago by ▴ 870
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Answer: A: extract data from txt files
updated 6.0 years ago by 45k • written 10.1 years ago by ▴ 870
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Answer: A: How can you convert a GATK interval_list file into a BED file
updated 6.0 years ago by 45k • written 10.4 years ago by ▴ 870
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Comment: C: The Biostar Handbook. A bioinformatics e-book for beginners.
8.9 years ago by Zaag ▴ 870
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217k
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Comment: C: The Biostar Handbook. A bioinformatics e-book for beginners.
8.9 years ago by Zaag ▴ 870
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217k
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Comment: C: The Biostar Handbook. A bioinformatics e-book for beginners.
8.9 years ago by Zaag ▴ 870
10
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Comment: C: The Biostar Handbook. A bioinformatics e-book for beginners.
8.9 years ago by Zaag ▴ 870
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Comment: C: Beginner in Python needs assistance with counting 'A's in DNA sequences
8.9 years ago by Zaag ▴ 870
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Comment: C: Beginner at Python- My task is to convert a FASTA file to a PHYLIP file (tab-del
8.9 years ago by Zaag ▴ 870
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Comment: C: python newbie - only else statement is printed
8.9 years ago by Zaag ▴ 870
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2.7k
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Answer: A: python newbie - only else statement is printed
8.9 years ago by Zaag ▴ 870
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2.7k
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Comment: C: python newbie - only else statement is printed
8.9 years ago by Zaag ▴ 870
0
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1
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4.4k
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Answer: A: Beginner at Python- My task is to convert a FASTA file to a PHYLIP file (tab-del
8.9 years ago by Zaag ▴ 870
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1
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5.3k
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Comment: C: Modifying Annovar Command Line: table_annovar.pl
8.9 years ago by Zaag ▴ 870
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2.8k
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Comment: C: Problems with proper interpretation of visualized bam file from Illumina Miniseq
8.9 years ago by Zaag ▴ 870
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2.8k
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Comment: C: Problems with proper interpretation of visualized bam file from Illumina Miniseq
8.9 years ago by Zaag ▴ 870
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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
8.9 years ago by Zaag ▴ 870
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2.3k
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Comment: C: Variant Calling problem - find alternate heterozygous
9.0 years ago by Zaag ▴ 870
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2.3k
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Answer: A: Variant Calling problem - find alternate heterozygous
9.0 years ago by Zaag ▴ 870
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2.4k
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Comment: C: Failing to use $mixin to include "global" settings
9.0 years ago by Zaag ▴ 870
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Answer: A: How can I get the exon number/rank of a mutation from annovar annotation?
9.0 years ago by Zaag ▴ 870
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Answer: A: use a input file to a mysql query to retrieve genomic coordinates from a list of
9.0 years ago by Zaag ▴ 870
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Comment: C: How to do context dependent data merge in python? help ?
9.0 years ago by Zaag ▴ 870
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2.8k
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Comment: C: bad quality reads with agilent panel on miseq
9.0 years ago by Zaag ▴ 870
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2.8k
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Comment: C: bad quality reads with agilent panel on miseq
9.0 years ago by Zaag ▴ 870
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1
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3.1k
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Comment: C: How to do context dependent data merge in python? help ?
9.0 years ago by Zaag ▴ 870
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1
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3.1k
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Answer: A: How to do context dependent data merge in python?
9.0 years ago by Zaag ▴ 870
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1
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2.4k
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Comment: C: Using 2 different references in my pipeline
9.0 years ago by Zaag ▴ 870
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7.3k
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Comment: C: Rmarkdown report from multiple images
9.0 years ago by Zaag ▴ 870
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7.3k
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Answer: A: Rmarkdown report from multiple images
9.0 years ago by Zaag ▴ 870
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Answer: A: Learning Python: list of resources
9.0 years ago by Zaag ▴ 870
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8.7k
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Comment: C: Please, please, define what a 'read' is.
9.0 years ago by Zaag ▴ 870
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8.7k
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Comment: C: Please, please, define what a 'read' is.
9.0 years ago by Zaag ▴ 870
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8.2k
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Comment: C: BWA and Soft clipping
9.0 years ago by Zaag ▴ 870
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3.2k
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Answer: A: IndelRealigner and RealignerTargetCreator for amplicon sequencing
9.0 years ago by Zaag ▴ 870
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5.5k
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Comment: C: Clinical significance explanation
9.0 years ago by Zaag ▴ 870
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Comment: C: Coverage analysis in a targeted amplicon-based next-generation sequencing panel
9.0 years ago by Zaag ▴ 870
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Comment: C: What are the most important unresolved problems in Bioinformatics?
9.0 years ago by Zaag ▴ 870
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2.8k
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Answer: A: Change vcf header in windows
9.0 years ago by Zaag ▴ 870
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1
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5.8k
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Answer: A: Coverage analysis in a targeted amplicon-based next-generation sequencing panel
9.1 years ago by Zaag ▴ 870
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4.7k
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Comment: C: I am trying to load a BAM file (Whole Genome) to IGV but I can't see anything
9.1 years ago by Zaag ▴ 870
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1
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3.0k
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Comment: C: NGS analysis with a core i3 laptop
9.2 years ago by Zaag ▴ 870
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1
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4.1k
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Comment: C: remove a percent of reads from a BAM file
9.2 years ago by Zaag ▴ 870
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4.1k
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Comment: C: remove a percent of reads from a BAM file
9.2 years ago by Zaag ▴ 870
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4.1k
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Answer: A: remove a percent of reads from a BAM file
9.2 years ago by Zaag ▴ 870
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8.7k
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Comment: C: dbsnp in vcf format compatible with hg38
9.2 years ago by Zaag ▴ 870
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1
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2.7k
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Answer: A: Remove few samples and their related information from dbSNP
9.2 years ago by Zaag ▴ 870
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Comment: C: Parallelizing SAMTOOLS: how to make my command run faster?
9.3 years ago by Zaag ▴ 870
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1
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2.1k
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Answer: A: Number of private variants/singletons in identical twins
9.3 years ago by Zaag ▴ 870
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