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| |style="color:black; background-color:#dcdcdc;" align="center"|Paper_title | | |style="color:black; background-color:#dcdcdc;" align="center"|Paper_title |
| |- | | |- |
− | |rowspan = "13"|2012/1/- | + | |rowspan = "2"|2012/2/21 |
| |align ="center"|2013-13 | | |align ="center"|2013-13 |
| |[http://www.nature.com/nbt/journal/v30/n11/full/nbt.2422.html (JE Shim, CY Kim) Interpreting noncoding genetic variation in complex traits and human disease] | | |[http://www.nature.com/nbt/journal/v30/n11/full/nbt.2422.html (JE Shim, CY Kim) Interpreting noncoding genetic variation in complex traits and human disease] |
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| |[http://genomebiology.com/2012/13/9/R48 (KS Kim, TH Kim) Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors] | | |[http://genomebiology.com/2012/13/9/R48 (KS Kim, TH Kim) Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors] |
| |- | | |- |
| + | |rowspan = "2"|2012/2/15 |
| |align ="center"|2013-11 | | |align ="center"|2013-11 |
| |[http://genome.cshlp.org/content/22/9/1798.long (ER Kim, HS Shim) Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors] | | |[http://genome.cshlp.org/content/22/9/1798.long (ER Kim, HS Shim) Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors] |
Line 17: |
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| |[http://genome.cshlp.org/content/22/9/1790.long (HJ Kim) Annotation of functional variation in personal genomes using RegulomeDB] | | |[http://genome.cshlp.org/content/22/9/1790.long (HJ Kim) Annotation of functional variation in personal genomes using RegulomeDB] |
| |- | | |- |
| + | |rowspan = "2"|2012/2/8 |
| |align ="center"|2013-09 | | |align ="center"|2013-09 |
| |[http://genome.cshlp.org/content/22/9/1775.long (HJ Kim) The GENCODE v7 catalog of human long noncoding RNAs: Analysis of their gene structure, evolution, and expression] | | |[http://genome.cshlp.org/content/22/9/1775.long (HJ Kim) The GENCODE v7 catalog of human long noncoding RNAs: Analysis of their gene structure, evolution, and expression] |
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| |[http://genome.cshlp.org/content/22/9/1760.long (HJ Kim) GENCODE: The reference human genome annotation for The ENCODE Project] | | |[http://genome.cshlp.org/content/22/9/1760.long (HJ Kim) GENCODE: The reference human genome annotation for The ENCODE Project] |
| |- | | |- |
| + | |rowspan = "2"|2012/2/1 |
| |align ="center"|2013-07 | | |align ="center"|2013-07 |
| |[http://genome.cshlp.org/content/22/9/1748.long (JE Shim, CY Kim) Linking disease associations with regulatory information in the human genome] | | |[http://genome.cshlp.org/content/22/9/1748.long (JE Shim, CY Kim) Linking disease associations with regulatory information in the human genome] |
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| |[http://genome.cshlp.org/content/22/9/1658.long (HJ Han, JH Kim) Understanding transcriptional regulation by integrative analysis of transcription factor binding data] | | |[http://genome.cshlp.org/content/22/9/1658.long (HJ Han, JH Kim) Understanding transcriptional regulation by integrative analysis of transcription factor binding data] |
| |- | | |- |
| + | |rowspan = "2"|2012/1/25 |
| |align ="center"|2013-05 | | |align ="center"|2013-05 |
| |[http://www.nature.com/nature/journal/v489/n7414/full/nature11233.html (ER Kim, HS Shim) Landscape of transcription in human cells] | | |[http://www.nature.com/nature/journal/v489/n7414/full/nature11233.html (ER Kim, HS Shim) Landscape of transcription in human cells] |
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| |[http://www.nature.com/nature/journal/v489/n7414/full/nature11245.html (HJ Han, JH Kim) Architecture of the human regulatory network derived from ENCODE data] | | |[http://www.nature.com/nature/journal/v489/n7414/full/nature11245.html (HJ Han, JH Kim) Architecture of the human regulatory network derived from ENCODE data] |
| |- | | |- |
| + | |rowspan = "2"|2012/1/18 |
| |align ="center"|2013-03 | | |align ="center"|2013-03 |
| |[http://www.nature.com/nature/journal/v489/n7414/full/nature11212.html (KS Kim, TH Kim) An expansive human regulatory lexicon encoded in transcription factor footprints] | | |[http://www.nature.com/nature/journal/v489/n7414/full/nature11212.html (KS Kim, TH Kim) An expansive human regulatory lexicon encoded in transcription factor footprints] |
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| |[http://www.nature.com/nature/journal/v489/n7414/full/nature11232.html (HJ Han, JH Kim) The accessible chromatin landscape of the human genome] | | |[http://www.nature.com/nature/journal/v489/n7414/full/nature11232.html (HJ Han, JH Kim) The accessible chromatin landscape of the human genome] |
| |- | | |- |
| + | |rowspan = "1"|2012/1/11 |
| |align ="center"|2012-01 | | |align ="center"|2012-01 |
| |[http://www.nature.com/nature/journal/v489/n7414/full/nature11247.html (JE Shim, CY Kim) An integrated encyclopedia of DNA elements in the human genome] | | |[http://www.nature.com/nature/journal/v489/n7414/full/nature11247.html (JE Shim, CY Kim) An integrated encyclopedia of DNA elements in the human genome] |
| |- | | |- |
− | |rowspan = "1"|2012/12/- | + | |rowspan = "1"|2012/1/11 |
| |align ="center"|2012-81 | | |align ="center"|2012-81 |
| |[http://genome.cshlp.org/content/22/8/1589.full (TH Kim) MuSiC: identifying mutational significance in cancer genomes.] | | |[http://genome.cshlp.org/content/22/8/1589.full (TH Kim) MuSiC: identifying mutational significance in cancer genomes.] |
Date
|
Paper_index
|
Paper_title
|
2012/2/21
|
2013-13
|
(JE Shim, CY Kim) Interpreting noncoding genetic variation in complex traits and human disease
|
2013-12
|
(KS Kim, TH Kim) Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors
|
2012/2/15
|
2013-11
|
(ER Kim, HS Shim) Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors
|
2013-10
|
(HJ Kim) Annotation of functional variation in personal genomes using RegulomeDB
|
2012/2/8
|
2013-09
|
(HJ Kim) The GENCODE v7 catalog of human long noncoding RNAs: Analysis of their gene structure, evolution, and expression
|
2013-08
|
(HJ Kim) GENCODE: The reference human genome annotation for The ENCODE Project
|
2012/2/1
|
2013-07
|
(JE Shim, CY Kim) Linking disease associations with regulatory information in the human genome
|
2013-06
|
(HJ Han, JH Kim) Understanding transcriptional regulation by integrative analysis of transcription factor binding data
|
2012/1/25
|
2013-05
|
(ER Kim, HS Shim) Landscape of transcription in human cells
|
2013-04
|
(HJ Han, JH Kim) Architecture of the human regulatory network derived from ENCODE data
|
2012/1/18
|
2013-03
|
(KS Kim, TH Kim) An expansive human regulatory lexicon encoded in transcription factor footprints
|
2013-02
|
(HJ Han, JH Kim) The accessible chromatin landscape of the human genome
|
2012/1/11
|
2012-01
|
(JE Shim, CY Kim) An integrated encyclopedia of DNA elements in the human genome
|
2012/1/11
|
2012-81
|
(TH Kim) MuSiC: identifying mutational significance in cancer genomes.
|
2012/12/04
|
2012-80
|
(CY KIM) Human genomic disease variants: A neutral evolutionary explanation
|
2012/11/20
|
2012-79
|
(HS Shim) Circuitry and Dynamics of Human Transcription Factor Regulatory Networks
|
2012-78
|
(HJ Kim) Interpreting cancer genomes using systematic host network perturbations by tumour virus proteins
|
2012/11/06
|
2012-77
|
(HJ Han) Systematic Localization of Common Disease-Associated Variation in Regulatory DNA
|
2012-76
|
(KS Kim) A public resource facilitating clinical use of genomes
|
2012/07/19
|
2012-75
|
(HJ Han & YH Ko) Predictive regulatory models in Drosophila melanogaster by integrative inference of transcriptional networks
|
2012-74
|
(JE Shim) An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People
|
2012-73
|
(JE Shim) Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
|
2012-72
|
(SH Hwang) Network-based classification of breast cancer metastasis
|
2012-71
|
(T Lee&CY Kim)Brain Expression Genome-Wide Association Study (eGWAS) Identifies Human Disease-Associated Variants
|
2012-70
|
(ER Kim&TH Kim)The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
|
2012/07/16
|
2012-69
|
(ER Kim&TH Kim)A framework for variation discovery and genotyping using next-generation DNA sequencing data
|
2012-66
|
(ER Kim&TH Kim)The Sequence Alignment/Map format and SAMtools
|
2012-65
|
(ER Kim&TH Kim)The Variant Call Format and VCFtools
|
2012-64
|
(YH Go&HJ Han)The Impact of the Gut Microbiota on Human Health: An Integrative View
|
2012-63
|
(T Lee&CY Kim)Host-Gut Microbiota Metabolic Interactions
|
2012-62
|
(AR Cho,JH Ju)Interactions Between the Microbiota and the Immune System
|
2012-61
|
(SH Hwang&HJ Cho)The Application of Ecological Theory Toward an Understanding of the Human Microbiome
|
2012-60
|
(SH Hwang&HJ Cho)Microbiota-Targeted Therapies: An Ecological Perspective
|
2012/07/13
|
2012-59
|
(JH Shin&HJ Kim)Metabolic Reconstruction for Metagenomic Data and Its Application to the Human Microbiome
|
2012-58
|
(JH Shin&HJ Kim)A framework for human microbiome research
|
2012-57
|
(JH Shin&HJ Kim)Structure, function and diversity of the healthy human microbiome
|
2012/07/12
|
2012-56
|
(AR Cho&JH Ju)COLT-Cancer: functional genetic screening resource for essential genes in human cancer cell lines
|
2012-55
|
(YH Go&HJ Han)Google Goes Cancer: Improving Outcome Prediction for Cancer Patients by Network-Based Ranking of Marker Genes
|
2012-54
|
(YH Go&HJ Han)A pharmacogenomic method for individualized prediction of drug sensitivity
|
2012-53
|
(JH Soh)The genomic and transcriptomic architecture of 2,000 breast tumours reveals novel subgroups
|
2012/07/09
|
2012-52
|
(ER Kim&TH Kim)The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
|
2012-51
|
(ER Kim&TH Kim)Systematic identification of genomic markers of drug sensitivity in cancer cells
|
2012-50
|
(ER Kim&TH Kim)Subtype and pathway specific responses to anticancer compounds in breast cancer
|
2012-49
|
(JE Shim&KS Kim)De novo mutations revealed by whole-exome sequencing are strongly associated with autism
|
2012-48
|
(JE Shim&KS Kim)Patterns and rates of exonic de novo mutations in autism spectrum disorders
|
2012-47
|
(JE Shim&KS Kim)Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
|
2012/07/06
|
2012-46
|
(T Lee&CY Kim)Integrating Rare-Variant Testing, Function Prediction, and Gene Network in Composite Resequencing-Based Genome-Wide Association Studies (CR-GWAS)
|
2012-45
|
(T Lee&CY Kim)Type 2 Diabetes Risk Alleles Demonstrate Extreme Directional Differentiation among Human Populations, Compared to Other Diseases
|
2012-44
|
(AR Cho&JH Ju)Predicting mutation outcome from early stochastic variation in genetic interaction partners
|
2012-43
|
(AR Cho&JH Ju)Fitness Trade-Offs and Environmentally Induced Mutation Buffering in Isogenic C. elegans
|
2012-42
|
(JE Shim&KS Kim)Identification of microRNA-regulated gene networks by expression analysis of target genes
|
2012-41
|
(JE Shim&KS Kim)Exome sequencing and the genetic basis of complex traits
|
2012/07/02
|
2012-40
|
(JH Soh)Functional Repurposing Revealed by Comparing S. pombe and S. cerevisiae Genetic Interactions
|
2012-39
|
(ER Kim&TH Kim)De novo discovery of mutated driver pathways in cancer
|
2012-38
|
(YH Go&HJ Han)A systems biology approach to prediction of oncogenes and molecular perturbation targets in B-cell lymphomas
|
2012-37
|
(SH Hwang&HJ Cho)PREDICT: a method for inferring novel drug indications with application to personalized medicine
|
2012-36
|
(SH Hwang&HJ Cho)Synergistic response to oncogenic mutations defines gene class critical to cancer phenotype
|
2012-35
|
(JH Shin&HJ Kim)Detecting Novel Associations in Large Data Sets
|
2012/03/05
|
2012-34
|
(8,HH Kim)Mapping and quantifying mammalian transcriptomes by RNA-Seq.
|
2012-33
|
(11,Go&Ju)Differential expression analysis for sequence count data
|
2012-32
|
(12,Go&Ju)edgeR: a Bioconductor package for differential expression analysis of digital gene expression data
|
2012/02/27 2012/02/28
|
2012-31
|
(1,JW Song)RNA-Seq: a revolutionary tool for transcriptomics
|
2012-30
|
(2,JW Song)Computational methods for transcriptome annotation and quantification using RNA-seq
|
2012-29
|
(3,HJ Han)From RNA-seq reads to differential expression results
|
2012-28
|
(4,AR Cho)Comprehensive comparative analysis of strand-specific RNA sequencing methods
|
2012-27
|
(5,T Lee)A Low-Cost Library Construction Protocol and Data Analysis Pipeline for Illumina-Based Strand-Specific Multiplex RNA-Seq
|
2012-26
|
(6,So&Shin)Transcript assembly and quantification by RNA-Seq reveals unannotated transcripts and isoform switching during cell differentiation
|
2012-25
|
(7,So&Shin)TopHat: discovering splice junctions with RNA-Seq
|
2012/02/06
|
2012-24
|
mirConnX: condition-specific mRNA-microRNA network integrator
|
2012-23
|
Construction and Analysis of an Integrated Regulatory Network Derived from High-Throughput Sequencing Data
|
2012-22
|
A Densely Interconnected Genome-Wide Network of MicroRNAs and Oncogenic Pathways Revealed Using Gene Expression Signatures
|
2012-21
|
Reprogramming of miRNA networks in cancer and leukemia
|
2012-20
|
An Extensive MicroRNA-Mediated Network of RNA-RNA Interactions Regulates Established Oncogenic Pathways in Glioblastoma
|
2012/01/30
|
2012-19
|
Principles and Strategies for Developing Network Models in Cancer
|
2012-18
|
Reverse engineering of regulatory networks in human B cells
|
2012-17
|
Variations in DNA elucidate molecular networks that cause disease
|
2012-16
|
Harnessing gene expression to identify the genetic basis of drug resistance
|
2012-15
|
An Integrated Approach to Uncover Drivers of Cancer
|
2012/01/09
|
2012-14
|
Genetic variation in an individual human exome.
|
2012-13
|
Predicting phenotypic variation in yeast from individual genome sequences.
|
2012-12
|
Clinical assessment incorporating a personal genome.
|
2012/01/09 2012/01/16
|
2012-11
|
Human allelic variation: perspective from protein function, structure, and evolution.
|
2012-10
|
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm.
|
2012-09
|
Prediction of deleterious human alleles.
|
2012-08
|
Human non-synonymous SNPs: server and survey.
|
2012-07
|
A method and server for predicting damaging missense mutations.
|
2012-06
|
SNAP: predict effect of non-synonymous polymorphisms on function
|
2012/01/09 2012/01/16
|
2012-05
|
Computational and statistical approaches to analyzing variants identified by exome sequencing.
|
2012-04
|
Shifting paradigm of association studies: value of rare single-nucleotide polymorphisms.
|
2012-03
|
Targeted capture and massively parallel sequencing of 12 human exomes.
|
2012/01/09 2012/01/16
|
2012-02
|
The distribution of fitness effects of new mutations.
|
2012-01
|
Most Rare Missense Alleles Are Deleterious in Humans: Implications for Complex Disease and Association Studies
|