(Q36478122)

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LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

high-throughput sequencing

1 reference

based on heuristic

inferred from title

object named as

Andreas Wilm

1

0 references

object named as

Swee Hoe Ong

5

0 references

Chiea Chuen Khor

object named as

Chiea Chuen Khor

7

0 references

Martin L. Hibberd

object named as

Martin Lloyd Hibberd

9

0 references

author name string

Pauline Poh Kim Aw

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Denis Bertrand

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Grace Hui Ting Yeo

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Chang Hua Wong

6

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Rosemary Petric

8

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Niranjan Nagarajan

10

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

language of work or name

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publication date

12 October 2012

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Europe PubMed Central

PMC publication ID

14 August 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

40

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

22

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

11189-11201

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

copyright license

Creative Commons Attribution-NonCommercial 3.0 Unported

5 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

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1 reference

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Noninvasive identification and monitoring of cancer mutations by targeted deep sequencing of plasma DNA.

1 reference

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Highly sensitive and specific detection of rare variants in mixed viral populations from massively parallel sequence data

1 reference

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Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing

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Clonal selection drives genetic divergence of metastatic medulloblastoma

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Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing

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1 reference

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1 reference

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Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study

1 reference

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1 reference

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Genotype and SNP calling from next-generation sequencing data

1 reference

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Sequence-specific error profile of Illumina sequencers

1 reference

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Mitochondrial subversion in cancer

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ShoRAH: estimating the genetic diversity of a mixed sample from next-generation sequencing data

1 reference

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Metabolic trade-offs and the maintenance of the fittest and the flattest

1 reference

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Beyond the consensus: dissecting within-host viral population diversity of foot-and-mouth disease virus by using next-generation genome sequencing

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Somatic mutations throughout the entire mitochondrial genome are associated with elevated PSA levels in prostate cancer patients.

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Massively parallel sequencing for monitoring genetic consistency and quality control of live viral vaccines

1 reference

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High-throughput discovery of rare insertions and deletions in large cohorts

1 reference

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Bacterial charity work leads to population-wide resistance

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Tumor heterogeneity is an active process maintained by a mutant EGFR-induced cytokine circuit in glioblastoma

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Quasispecies theory and the behavior of RNA viruses

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

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A statistical method for the detection of variants from next-generation resequencing of DNA pools

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Rhinovirus genome evolution during experimental human infection

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1093/NAR/GKS918

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

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