| P50 | author | Raúl Rabadán | Q7296181 |
| | Hossein Khiabanian | Q55167918 |
| | Laura Pasqualucci | Q30303485 |
| P2093 | author name string | Gyan Bhanot | |
| | Nicholas Chiorazzi | |
| | Sonia Marsilio | |
| P2860 | cites work | Mutational and structural analysis of diffuse large B-cell lymphoma using whole-genome sequencing | Q37098851 |
| | Clinical impact of small subclones harboring NOTCH1, SF3B1 or BIRC3 mutations in chronic lymphocytic leukemia | Q37216310 |
| | How tumours escape mass destruction | Q37287162 |
| | Mutational landscape, clonal evolution patterns, and role of RAS mutations in relapsed acute lymphoblastic leukemia | Q37322911 |
| | ERIC recommendations on TP53 mutation analysis in chronic lymphocytic leukemia | Q37980658 |
| | Origins of lymphatic and distant metastases in human colorectal cancer. | Q38373329 |
| | Clinical Implications of Novel Genomic Discoveries in Chronic Lymphocytic Leukemia | Q38744632 |
| | Subclonal variant calling with multiple samples and prior knowledge | Q38940323 |
| | DNA damage is a pervasive cause of sequencing errors, directly confounding variant identification. | Q38956391 |
| | Integrating liquid biopsies into the management of cancer | Q39157824 |
| | Clonal evolution of glioblastoma under therapy. | Q39704836 |
| | Multiplex Real-Time PCR Assays that Measure the Abundance of Extremely Rare Mutations Associated with Cancer | Q41986671 |
| | Universal Patterns of Selection in Cancer and Somatic Tissues | Q46278243 |
| | Somatic CLL mutations occur at multiple distinct hematopoietic maturation stages: documentation and cautionary note regarding cell fraction purity | Q50081106 |
| | Reliable detection of subclonal single-nucleotide variants in tumour cell populations. | Q51372620 |
| | Tracing the origins of relapse in acute myeloid leukaemia to stem cells. | Q51838074 |
| | Chronic lymphocytic leukaemia | Q56270980 |
| | Robustness of Amplicon Deep Sequencing Underlines Its Utility in Clinical Applications | Q57740675 |
| | Mutations of Bacteria from Virus Sensitivity to Virus Resistance | Q24533278 |
| | Fast and accurate short read alignment with Burrows-Wheeler transform | Q24653853 |
| | PCR-based methods for the enrichment of minority alleles and mutations | Q24657701 |
| | ABT-199, a potent and selective BCL-2 inhibitor, achieves antitumor activity while sparing platelets | Q27683708 |
| | Assessment of Minimal Residual Disease in Standard-Risk AML. | Q27853325 |
| | Clinical impact of clonal and subclonal TP53, SF3B1, BIRC3, NOTCH1, and ATM mutations in chronic lymphocytic leukemia. | Q27853333 |
| | Chronic lymphocytic leukemia: 2015 Update on diagnosis, risk stratification, and treatment | Q28082086 |
| | Integrated mutational and cytogenetic analysis identifies new prognostic subgroups in chronic lymphocytic leukemia | Q28394721 |
| | Viral diversity and clonal evolution from unphased genomic data. | Q30370595 |
| | Detecting ultralow-frequency mutations by Duplex Sequencing | Q30413211 |
| | Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation | Q30455659 |
| | Detection and quantification of rare mutations with massively parallel sequencing | Q30472217 |
| | An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data | Q30597080 |
| | An empirical Bayes method for genotyping and SNP detection using multi-sample next-generation sequencing data | Q31112462 |
| | Clinical impact of small TP53 mutated subclones in chronic lymphocytic leukemia | Q33595764 |
| | Kinetic hairpin oligonucleotide blockers for selective amplification of rare mutations | Q33985749 |
| | A new approach for detecting low-level mutations in next-generation sequence data | Q34279191 |
| | PEAR: a fast and accurate Illumina Paired-End reAd mergeR. | Q34379012 |
| | Tumor evolutionary directed graphs and the history of chronic lymphocytic leukemia | Q34453174 |
| | Integrated digital error suppression for improved detection of circulating tumor DNA | Q34520008 |
| | Ultra-deep mutant spectrum profiling: improving sequencing accuracy using overlapping read pairs | Q34583054 |
| | Emerging landscape of oncogenic signatures across human cancers | Q35058708 |
| | SAVI: a statistical algorithm for variant frequency identification | Q35101975 |
| | Chromatin conformation governs T-cell receptor Jβ gene segment usage | Q36300640 |
| | Ibrutinib as Initial Therapy for Patients with Chronic Lymphocytic Leukemia | Q36490049 |
| | Tumor cells can follow distinct evolutionary paths to become resistant to epidermal growth factor receptor inhibition | Q36989342 |
| | Large population solution of the stochastic Luria-Delbruck evolution model | Q37031674 |
| | Rates and mechanisms of bacterial mutagenesis from maximum-depth sequencing | Q37083023 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | statistics | Q12483 |
| P6104 | maintained by WikiProject | WikiProject Mathematics | Q8487137 |
| P304 | page(s) | 143-155 | |
| P577 | publication date | 2018-07-01 | |
| P1433 | published in | Journal of Statistical Physics | Q1878468 |
| P1476 | title | On statistical modeling of sequencing noise in high depth data to assess tumor evolution | |
| P478 | volume | 172 | |