56 results on '"Lee, Choli"'
Search Results
2. Chromatin context-dependent regulation and epigenetic manipulation of prime editing
3. Chromatin context-dependent regulation and epigenetic manipulation of prime editing
4. Multiplex profiling of developmental enhancers with quantitative, single-cell expression reporters
5. A time-resolved, multi-symbol molecular recorder via sequential genome editing
6. Multiplex genomic recording of enhancer and signal transduction activities in mammalian cells
7. Multiplex genomic recording of enhancer and signal transduction activity in mammalian cells
8. A temporally resolved, multiplex molecular recorder based on sequential genome editing
9. Precise genomic deletions using paired prime editing
10. Single-cell landscape of nuclear configuration and gene expression during stem cell differentiation and X inactivation
11. Precise genomic deletions using paired prime editing
12. A Three-Dimensional Model of the Yeast Genome
13. Single-cell landscape of nuclear configuration and gene expression during stem cell differentiation and X inactivation
14. TransMPRA: A framework for assaying the role of many trans-acting factors at many enhancers
15. Unsupervised manifold alignment for single-cell multi-omics data
16. Capturing cell type-specific chromatin compartment patterns by applying topic modeling to single-cell Hi-C data
17. Sci-Hi-C: A single-cell Hi-C method for mapping 3D genome organization in large number of single cells
18. Sci-Hi-C: a single-cell Hi-C method for mapping 3D genome organization in large number of single cells
19. Capturing cell type-specific chromatin structural patterns by applying topic modeling to single-cell Hi-C data
20. A Single-Cell Atlas of In Vivo Mammalian Chromatin Accessibility
21. Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution
22. Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
23. Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution
24. Comprehensive single-cell transcriptional profiling of a multicellular organism
25. CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic Deletions
26. Correction: A Year of Infection in the Intensive Care Unit: Prospective Whole Genome Sequencing of Bacterial Clinical Isolates Reveals Cryptic Transmissions and Novel Microbiota
27. Comprehensive statistical inference of the clonal structure of cancer from multiple biopsies
28. Comprehensive single cell transcriptional profiling of a multicellular organism by combinatorial indexing
29. Paired CRISPR/Cas9 guide-RNAs enable high-throughput deletion scanning (ScanDel) of a Mendelian disease locus for functionally critical non-coding elements
30. Recurrent somatic loss ofTNFRSF14in classical Hodgkin lymphoma
31. A Year of Infection in the Intensive Care Unit: Prospective Whole Genome Sequencing of Bacterial Clinical Isolates Reveals Cryptic Transmissions and Novel Microbiota
32. Whole genome prediction for preimplantation genetic diagnosis
33. Fine-scale chromatin interaction maps reveal the cis-regulatory landscape of human lincRNA genes
34. Deep sequencing of multiple regions of glial tumors reveals spatial heterogeneity for mutations in clinically relevant genes
35. Large-scale genomic sequencing of extraintestinal pathogenic Escherichia coli strains
36. Whole-Genome Sequencing of Individuals from a Founder Population Identifies Candidate Genes for Asthma
37. The haplotype-resolved genome and epigenome of the aneuploid HeLa cancer cell line
38. Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders
39. A genome-wide 3C-method for characterizing the three-dimensional architectures of genomes
40. Accurate gene synthesis with tag-directed retrieval of sequence-verified DNA molecules
41. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
42. Resolving the Breakpoints of the 17q21.31 Microdeletion Syndrome with Next-Generation Sequencing
43. Abstract 5059: Exome and targeted sequencing to discover and validate candidate genes in advanced and lethal prostate cancer
44. Erratum: Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
45. Massively parallel functional dissection of mammalian enhancers in vivo
46. Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers
47. Gorilla genome structural variation reveals evolutionary parallelisms with chimpanzee
48. Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations
49. Biome representational in silico karyotyping
50. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.