genome analysis toolkit software package version 1.6 (Broad Institute Inc)
90
Structured Review
Broad Institute Inc
genome analysis toolkit software package version 1.6
Genome Analysis Toolkit Software Package Version 1.6, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/genome+analysis+toolkit+software+package+version+1%2E6/genome+analysis+toolkit+software+package+version+1+6/pmc10466493-172-0-8
Average 90 stars, based on 1 article reviews
Genome Analysis Toolkit Software Package Version 1.6, supplied by Broad Institute Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/genome+analysis+toolkit+software+package+version+1%2E6/genome+analysis+toolkit+software+package+version+1+6/pmc10466493-172-0-8
Average 90 stars, based on 1 article reviews
genome analysis toolkit software package version 1.6 - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
Software:Article Title: Long-range PCR amplification-based targeted enrichment & next generation sequencing: A cost-effective testing strategy for lysosomal storage disorders Article Snippet: Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA, USA) was used for variant calling and ANNOVAR software version 2012 was used for annotation of the variants . Article Title: Molecular Diagnosis of Autosomal Dominant Polycystic Kidney Disease Using Next-Generation Sequencing Article Snippet: Sequence variants were called using the Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA), 24 carefully following the best practice guidelines recommended by GATK, 25 including initial read mapping, local realignment particularly around indels, followed by base quality score recalibration. Article Title: Molecular diagnosis of autosomal dominant polycystic kidney disease using next-generation sequencing. Article Snippet: Sequence variants were called using the Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA),24 carefully following the best practice guidelines recommended by GATK,25 including initial read mapping, local realignment particularly around indels, followed by base quality score recalibration. Variant Assay:Article Title: Long-range PCR amplification-based targeted enrichment & next generation sequencing: A cost-effective testing strategy for lysosomal storage disorders Article Snippet: Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA, USA) was used for variant calling and ANNOVAR software version 2012 was used for annotation of the variants . Article Title: Molecular Diagnosis of Autosomal Dominant Polycystic Kidney Disease Using Next-Generation Sequencing Article Snippet: Sequence variants were called using the Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA), 24 carefully following the best practice guidelines recommended by GATK, 25 including initial read mapping, local realignment particularly around indels, followed by base quality score recalibration. Article Title: Molecular diagnosis of autosomal dominant polycystic kidney disease using next-generation sequencing. Article Snippet: Sequence variants were called using the Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA),24 carefully following the best practice guidelines recommended by GATK,25 including initial read mapping, local realignment particularly around indels, followed by base quality score recalibration. Sequencing:Article Title: Long-range PCR amplification-based targeted enrichment & next generation sequencing: A cost-effective testing strategy for lysosomal storage disorders Article Snippet: Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA, USA) was used for variant calling and ANNOVAR software version 2012 was used for annotation of the variants . Article Title: Molecular Diagnosis of Autosomal Dominant Polycystic Kidney Disease Using Next-Generation Sequencing Article Snippet: Sequence variants were called using the Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA), 24 carefully following the best practice guidelines recommended by GATK, 25 including initial read mapping, local realignment particularly around indels, followed by base quality score recalibration. Article Title: Molecular diagnosis of autosomal dominant polycystic kidney disease using next-generation sequencing. Article Snippet: Sequence variants were called using the Genome Analysis Toolkit (GATK) software package version 1.6 (Broad Institute, Cambridge, MA),24 carefully following the best practice guidelines recommended by GATK,25 including initial read mapping, local realignment particularly around indels, followed by base quality score recalibration. |