ERRATUM: Acknowledgments Correction. Bioinformatics Interpretation of Exome Sequencing: Blood Cancer

ERRATUM: Acknowledgments Correction. Bioinformatics Interpretation of Exome Sequencing: Blood Cancer

Saved in:

Bibliographic Details
Main Authors:	Jiwoong Kim, Yun-Gyeong Lee, Namshin Kim
Format:	Article
Language:	English
Published:	BioMed Central 2013-06-01
Series:	Genomics & Informatics
Online Access:	http://genominfo.org/upload/pdf/gni-11-98.pdf
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Bioinformatics Interpretation of Exome Sequencing: Blood Cancer
by: Jiwoong Kim, et al.
Published: (2013-03-01)

ERRATUM: Acknowledgments Correction. Annotation of Genes Having Candidate Somatic Mutations in Acute Myeloid Leukemia with Whole-Exome Sequencing Using Concept Lattice Analysis
by: Kye Hwa Lee, et al.
Published: (2013-06-01)

ERRATUM: Acknowledgments Correction. Cell-Free miR-27a, a Potential Diagnostic and Prognostic Biomarker for Gastric Cancer
by: Jong-Lyul Park, et al.
Published: (2015-12-01)

Computational and Bioinformatics Frameworks for Next-Generation Whole Exome and Genome Sequencing
by: Marisa P. Dolled-Filhart, et al.
Published: (2013-01-01)

Effect of Next-Generation Exome Sequencing Depth for Discovery of Diagnostic Variants
by: Kyung Kim, et al.
Published: (2015-06-01)

Validity of patient-derived xenograft mouse models for lung cancer based on exome sequencing data
by: Jaewon Kim, et al.
Published: (2020-03-01)

Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer
by: Kyong-Ah Yoon, et al.
Published: (2018-12-01)

Acknowledgements
by: Francois P. Retief, et al.
Published: (2005-06-01)

Acknowledgements
by: Engaged Scholar Journal
Published: (2025-01-01)

Exome sequencing of 18,994 ethnically diverse patients with suspected rare Mendelian disorders
by: Heonjong Han, et al.
Published: (2025-01-01)

Correction: Exome sequencing reveals IFT172 variants in patients with non-syndromic cholestatic liver disease.
by: Magdaléna Neřoldová, et al.
Published: (2025-01-01)

Whole exome sequencing enables the correct diagnosis of Frank–Ter Haar syndrome in a Saudi family
by: Y. N. Khan, et al.
Published: (2024-05-01)

Whole exome sequencing identifies genomic alterations in proximal and distal colorectal cancer
by: Ryia-Illani Mohd Yunos, et al.
Published: (2019-09-01)

Acknowledgement to reviewers
by: Editorial Office
Published: (2024-11-01)

Acknowledgement to reviewers
by: Editorial Office
Published: (2024-11-01)

Acknowledgement to reviewers
by: Editorial Office
Published: (2024-11-01)

Acknowledgement to Reviewers
Published: (2025-01-01)

ACKNOWLEDGMENT TO REVIEWERS
Published: (2024-02-01)

Acknowledgement of reviewers
Published: (2025-12-01)

Summary and acknowledgements
by: Róbert Sinka
Published: (2009-06-01)

Preface and Acknowledgements
by: Anne-Marie Kilday and Nathalie Vanfasse
Published: (2005-12-01)

Reviewer acknowledgement
by: Chloe E. H. Scott
Published: (2025-01-01)

Reviewer acknowledgement
by: Fares S. Haddad
Published: (2025-01-01)

Whole Exome Sequencing Uncovers Germline Variants of Cancer-Related Genes in Sporadic Pheochromocytoma
by: Milena Urbini, et al.
Published: (2018-01-01)

Whole exome sequencing-based homologous recombination deficiency test for epithelial ovarian cancer
by: Ying-Cheng Chiang, et al.
Published: (2025-01-01)

Revealing Genomic Profile That Underlies Tropism of Myeloma Cells Using Whole Exome Sequencing
by: Youngil Koh, et al.
Published: (2015-01-01)

Exome sequencing in Nigerian children with early‐onset epilepsy syndromes
by: Ibitayo Abigail Ademuwagun, et al.
Published: (2025-02-01)

Diagnostic efficiency of exome-based sequencing in pediatric patients with epilepsy
by: Huafang Zou, et al.
Published: (2025-01-01)

Annotation of Genes Having Candidate Somatic Mutations in Acute Myeloid Leukemia with Whole-Exome Sequencing Using Concept Lattice Analysis
by: Kye Hwa Lee, et al.
Published: (2013-03-01)

Acknowledgements of Reviewers in 2024
Published: (2025-01-01)

Bioinformatics services for analyzing massive genomic datasets
by: Gunhwan Ko, et al.
Published: (2020-03-01)

An Atypical Presentation of Pyridoxine-Dependent Epilepsy Diagnosed with Whole Exome Sequencing and Treated with Lysine Restriction and Supplementation with Arginine and Pyridoxine
by: Jiyoung Kim, et al.
Published: (2022-01-01)

Multilocus Sequence Typing for Interpreting Blood Isolates of Staphylococcus epidermidis
by: Prannda Sharma, et al.
Published: (2014-01-01)

Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing
by: Ahmed Bouhouche, et al.
Published: (2018-01-01)

Application of copy number variation sequencing combined with whole exome sequencing in prenatal left–right asymmetry disorders
by: Yu Qin, et al.
Published: (2025-01-01)

ERRATUM: Author's Affiliation Correction. Heritabilities of Facial Measurements and Their Latent Factors in Korean Families
by: Hyun-Jin Kim, et al.
Published: (2013-09-01)

2024 Acknowledgment of mBio Reviewers
by: Arturo Casadevall
Published: (2025-02-01)

Trio-based whole-exome sequencing reveals mutations in early-onset high myopia
by: Ding Chen, et al.
Published: (2024-05-01)

Application of Whole Exome Sequencing to Identify Disease-Causing Variants in Inherited Human Diseases
by: Gerald Goh, et al.
Published: (2012-12-01)

Whole Exome Sequencing Reveals Rare Variants in Genes Associated with Metabolic Disorders in Women with PCOS
by: Priyal Sharma, et al.
Published: (2023-10-01)