Oncohematology

Twist custom panels are highly customisable solutions, allowing the exact selection of regions, genes, pathways or variants of interest. They are designed to offer high performance, flexibility and precision in all types of applications and starting samples. Detailed Description Operating principle: In practice, the use of custom panels makes it possible to overcome the limitations…

Advanced cloud-based bioinformatics platform designed for the automated analysis, interpretation, and classification of somatic variants in oncology. Through an integrated environment, the system evaluates clinical evidence in real time, automates classification in accordance with AMP/ASCO/CAP guidelines, and provides access to currently active clinical trials. Detailed description Operating principle End-to-end cloud-based solution for the clinical interpretation…

SeqOne is a bioinformatics platform for NGS data analysis in precision oncology, designed to detect, prioritise and interpret somatic variants and generate actionable clinical reports from raw sequencing data. It helps laboratories and healthcare professionals accelerate the interpretation of NGS data through an end-to-end workflow. Detailed description Operating principle SeqOne Genomics is a genomic data…

Franklin by QIAGEN is a cloud-based bioinformatics platform designed for the management, analysis, and interpretation of human genomic data. The solution centralizes case evaluation, quality control, variant prioritization, and classification into a structured workflow, facilitating the review and interpretation of complex sequencing data for specialized professionals. Detailed Description This cloud-based bioinformatics software has been developed…

Dr. PCR™ BCR-ABL1 Major IS Detection Kit is an in vitro diagnostic solution designed for monitoring patients with Chronic Myeloid Leukemia (CML). The kit is designed for the quantification of BCR-ABL1 (e13a2 and e14a2) and ABL1 transcripts from RNA extracted from whole blood. This is a digital PCR technology that stands out for its simplicity,…

NGS panel for the study of 23 key genes associated with Chronic Lymphocytic Leukemia (CLL), including the biomarkers outlined in international guidelines (TP53 and somatic hypermutation).

Chimerism monitoring by NGS

NGS kit for chimerism assessment

Study of 54 genes associated with different types of lymphomas.

Archer Immunoverse

NGS panel for the study of fusions, point mutations and expression levels in lymphomes.

NGS panel for the study of fusions, point mutations and expression levels in several types of myeloid diseases.

NGS analysis of relevant regions related to Acute Lymphoblastic Leukemia.

Detection of chromosomal aberrations in acute myeloid leukemia (AML).

Multiplex-PCR assay to identify informative polymorphisms for chimerism analysis.

Quantitative analysis of chimerism with specific insertion/deletion polimorfisms.

Kit for chimerism monitoring after bone marrow transplantation.

Identification of mutations associated to Myelodysplasic Syndroms, Myeloproliferative Neoplasms and Leukemia.