CLL-seq

This little twitterbot collects papers on CLL, focusing on next generation sequencing data

[CLL-seq @CLLseq]

Comprehensive Childhood ALL Genotyping May Optimize Risk Stratification https://t.co/qEjkOrlSTA

[CLL-seq @CLLseq]

Targeted Sequencing Adds Value to FISH for Detecting Genetic Alterations in CLL https://t.co/04LX6UgUKA

[CLL-seq @CLLseq]

Common and rare variants in genetic susceptibility analysis of mature B-cell neoplasm ... https://t.co/1fyCo6HJLt

[CLL-seq @CLLseq]

Why whole genome sequencing can improve child cancer treatments - Yahoo News UK https://t.co/cPNsRKmkAH

[CLL-seq @CLLseq]

IMS scientists received the 2023 RIKEN EIHO and RIKEN BAIHO Awards https://t.co/ppU5zZFOdi

[CLL-seq @CLLseq]

Patients With MPNs Have Increased Risk of Thrombosis, Hemorrhage, Leukemic Transformation https://t.co/zQswzglrkP

[CLL-seq @CLLseq]

Molecular Mapping of CLL and Richter Syndrome Offers Crucial Insights https://t.co/PEtf6hNr86

[CLL-seq @CLLseq]

New genomic classification of pediatric acute myeloid leukemia | Nature Genetics https://t.co/4aPhMcsJYq

[CLL-seq @CLLseq]

A new genomic framework to categorize pediatric acute myeloid leukemia | Nature Genetics https://t.co/9c12bH4I3w

[CLL-seq @CLLseq]

Chronic Lymphocytic Leukemia IGHV Somatic Hypermutation Detection by Targeted Capture Next-Generation Sequencing https://t.co/c7ZkucWktQ

[CLL-seq @CLLseq]

Genetic predisposition to differentiated thyroid cancer among Polish population https://t.co/fqXJQeiN7U

[CLL-seq @CLLseq]

Improved detection of clinically relevant fusion transcripts in cancer by machine learning classification https://t.co/v1dJGxpQYZ

[CLL-seq @CLLseq]

HYENA detects oncogenes activated by distal enhancers in cancer https://t.co/dpy9DXty3C

[CLL-seq @CLLseq]

Integrative NGS testing reveals clonal dynamics of adverse genomic defects contributing to a natural progression in treatment-naïve CLL patients https://t.co/TqnWXYU2Zt

[CLL-seq @CLLseq]

Incorporating mutational heterogeneity to identify genes that are enriched for synonymous mutations in cancer https://t.co/zufokbiLti

[CLL-seq @CLLseq]

Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia https://t.co/UkjEQ1tT8O

[CLL-seq @CLLseq]

Noncoding mutations cause super-enhancer retargeting resulting in protein synthesis dysregulation during B cell lymphoma progression https://t.co/oAPKcgFltN

[CLL-seq @CLLseq]

Low-burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation https://t.co/qk77N5EZQ8

[CLL-seq @CLLseq]

Applications and analysis of targeted genomic sequencing in cancer studies https://t.co/azWIRAVKKZ

[CLL-seq @CLLseq]

Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases https://t.co/Aoa7mOJ947