novoalign version 3.02.13 (Thermo Fisher)
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Thermo Fisher
novoalign version 3.02.13
Novoalign Version 3.02.13, supplied by Thermo Fisher, 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/novoalign/pm39806575-34-6-17
Average 90 stars, based on 1 article reviews
Novoalign Version 3.02.13, supplied by Thermo Fisher, 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/novoalign/pm39806575-34-6-17
Average 90 stars, based on 1 article reviews
novoalign version 3.02.13 - by Bioz Stars,
2026-09
90/100 stars
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Sequencing:Article Title: Leukemia relapse via genetic immune escape after allogeneic hematopoietic cell transplantation Article Snippet: .. Details of the bioinformatic approach to investigate somatic HLA mutational status have been described elsewhere.14 In brief, after obtaining a confident full 4th field typing through NovoHLA typing algorithm (Novocraft Technologies), paired-end reads from either targeting sequencing were directly aligned on a per-patient HLA reference using Article Title: Prevalence of TTR variants detected by whole-exome sequencing in hypertrophic cardiomyopathy. Article Snippet: Exome sequencing of the enriched libraries occurred on the Illumina Hiseq4000 platform at a minimum of 30 coverage, using standard manufacturer’s protocols. .. Sequence reads alignment against the reference human genome (UCSC hg19) was performed using Article Title: Leukemia relapse via genetic immune escape after allogeneic hematopoietic cell transplantation Article Snippet: Severity of acute GvHD was graded according to Glucksberg’s criteria5 whereas the assessment of all patients developing chronic GVHD was made according to the National Institute of Health (NIH) consensus criteria.6,7 DNA isolation Genomic DNA was isolated directly from cryopreserved unfractionated peripheral or bone marrow blood mononuclear cells with the Nuclei Lysis Solution (Promega) according to manufacturer’s instructions. .. HLA mutational analysis Details of the bioinformatic approach to investigate somatic HLA mutational status have been described elsewhere.8 In brief, after obtaining a confident full 4th field typing through NovoHLA typing algorithm (Novocraft Technologies), paired-end reads from either targeting sequencing were directly aligned on a per-patient HLA reference using Software:Article Title: Verification of Underlying Genetic Cause in a Cohort of Russian Patients with Familial Hypercholesterolemia Using Targeted Next Generation Sequencing Article Snippet: Sequencing was performed using the Illumina HiSeq 1500 platform (Illumina, San Diego, CA, USA) with 2 × 100 base pair read length following Illumina protocols. .. Bioinformatics analysis was performed by means of a custom pipeline that includes software as Variant Assay:Article Title: Verification of Underlying Genetic Cause in a Cohort of Russian Patients with Familial Hypercholesterolemia Using Targeted Next Generation Sequencing Article Snippet: Sequencing was performed using the Illumina HiSeq 1500 platform (Illumina, San Diego, CA, USA) with 2 × 100 base pair read length following Illumina protocols. .. Bioinformatics analysis was performed by means of a custom pipeline that includes software as |
