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  1. Article: Modeling interpretable correspondence between cell state and perturbation response with CellCap.

    Xu, Yang / Fleming, Stephen / Tegtmeyer, Matthew / McCarroll, Steven A / Babadi, Mehrtash

    bioRxiv : the preprint server for biology

    2024  

    Abstract: Single-cell transcriptomics, in conjunction with genetic and compound perturbations, offers a robust approach for exploring cellular behaviors in diverse contexts. Such experiments allow uncovering cell-state-specific responses to perturbations, a ... ...

    Abstract Single-cell transcriptomics, in conjunction with genetic and compound perturbations, offers a robust approach for exploring cellular behaviors in diverse contexts. Such experiments allow uncovering cell-state-specific responses to perturbations, a crucial aspect in unraveling the intricate molecular mechanisms governing cellular behavior and potentially discovering novel regulatory pathways and therapeutic targets. However, prevailing computational methods predominantly focus on predicting average cellular responses, disregarding the inherent response heterogeneity associated with cell state diversity. In this study, we present CellCap, a deep generative model designed for the end-to-end analysis of single-cell perturbation experiments. CellCap employs sparse dictionary learning in a latent space to deconstruct cell-state-specific perturbation responses into a set of transcriptional response programs. These programs are then utilized by each perturbation condition and each cell at varying degrees. The incorporation of specific model design choices, such as dot-product cross-attention between cell states and response programs, along with a linearly-decoded latent space, underlay the interpretation power of CellCap. We evaluate CellCap's model interpretability through multiple simulated scenarios and apply it to two real single-cell perturbation datasets. These datasets feature either heterogeneous cellular populations or a complex experimental setup. Our results demonstrate that CellCap successfully uncovers the relationship between cell state and perturbation response, unveiling novel insights overlooked in previous analyses. The model's interpretability, coupled with its effectiveness in capturing heterogeneous responses, positions CellCap as a valuable tool for advancing our understanding of cellular behaviors in the context of perturbation experiments.
    Language English
    Publishing date 2024-03-16
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.03.14.585078
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies.

    Genovese, Giulio / Rockweiler, Nicole B / Gorman, Bryan R / Bigdeli, Tim B / Pato, Michelle T / Pato, Carlos N / Ichihara, Kiku / McCarroll, Steven A

    Bioinformatics (Oxford, England)

    2024  Volume 40, Issue 2

    Abstract: Motivation: Many genetics studies report results tied to genomic coordinates of a legacy genome assembly. However, as assemblies are updated and improved, researchers are faced with either realigning raw sequence data using the updated coordinate system ...

    Abstract Motivation: Many genetics studies report results tied to genomic coordinates of a legacy genome assembly. However, as assemblies are updated and improved, researchers are faced with either realigning raw sequence data using the updated coordinate system or converting legacy datasets to the updated coordinate system to be able to combine results with newer datasets. Currently available tools to perform the conversion of genetic variants have numerous shortcomings, including poor support for indels and multi-allelic variants, that lead to a higher rate of variants being dropped or incorrectly converted. As a result, many researchers continue to work with and publish using legacy genomic coordinates.
    Results: Here we present BCFtools/liftover, a tool to convert genomic coordinates across genome assemblies for variants encoded in the variant call format with improved support for indels represented by different reference alleles across genome assemblies and full support for multi-allelic variants. It further supports variant annotation fields updates whenever the reference allele changes across genome assemblies. The tool has the lowest rate of variants being dropped with an order of magnitude less indels dropped or incorrectly converted and is an order of magnitude faster than other tools typically used for the same task. It is particularly suited for converting variant callsets from large cohorts to novel telomere-to-telomere assemblies as well as summary statistics from genome-wide association studies tied to legacy genome assemblies.
    Availability and implementation: The tool is written in C and freely available under the MIT open source license as a BCFtools plugin available at http://github.com/freeseek/score.
    MeSH term(s) Software ; Genome-Wide Association Study ; Genomics/methods ; Alleles ; INDEL Mutation
    Language English
    Publishing date 2024-01-23
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 1422668-6
    ISSN 1367-4811 ; 1367-4803
    ISSN (online) 1367-4811
    ISSN 1367-4803
    DOI 10.1093/bioinformatics/btae038
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Monogenic and polygenic inheritance become instruments for clonal selection.

    Loh, Po-Ru / Genovese, Giulio / McCarroll, Steven A

    Nature

    2020  Volume 584, Issue 7819, Page(s) 136–141

    Abstract: Clonally expanded blood cells that contain somatic mutations (clonal haematopoiesis) are commonly acquired with age and increase the risk of blood ... ...

    Abstract Clonally expanded blood cells that contain somatic mutations (clonal haematopoiesis) are commonly acquired with age and increase the risk of blood cancer
    MeSH term(s) Adult ; Aged ; Alleles ; Cardiovascular Diseases/genetics ; Cardiovascular Diseases/pathology ; Cell Division/genetics ; Chromosome Aberrations ; Clonal Evolution/genetics ; Clone Cells/cytology ; Clone Cells/metabolism ; Clone Cells/pathology ; Female ; Genetic Predisposition to Disease ; Hematologic Neoplasms/genetics ; Hematologic Neoplasms/pathology ; Hematopoiesis/genetics ; Humans ; Loss of Heterozygosity/genetics ; Male ; Middle Aged ; Mosaicism ; Multifactorial Inheritance/genetics ; United Kingdom
    Language English
    Publishing date 2020-06-24
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 120714-3
    ISSN 1476-4687 ; 0028-0836
    ISSN (online) 1476-4687
    ISSN 0028-0836
    DOI 10.1038/s41586-020-2430-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer.

    Mukamel, Ronen E / Handsaker, Robert E / Sherman, Maxwell A / Barton, Alison R / Hujoel, Margaux L A / McCarroll, Steven A / Loh, Po-Ru

    Cell

    2023  Volume 186, Issue 17, Page(s) 3659–3673.e23

    Abstract: Many regions in the human genome vary in length among individuals due to variable numbers of tandem repeats (VNTRs). To assess the phenotypic impact of VNTRs genome-wide, we applied a statistical imputation approach to estimate the lengths of 9,561 ... ...

    Abstract Many regions in the human genome vary in length among individuals due to variable numbers of tandem repeats (VNTRs). To assess the phenotypic impact of VNTRs genome-wide, we applied a statistical imputation approach to estimate the lengths of 9,561 autosomal VNTR loci in 418,136 unrelated UK Biobank participants and 838 GTEx participants. Association and statistical fine-mapping analyses identified 58 VNTRs that appeared to influence a complex trait in UK Biobank, 18 of which also appeared to modulate expression or splicing of a nearby gene. Non-coding VNTRs at TMCO1 and EIF3H appeared to generate the largest known contributions of common human genetic variation to risk of glaucoma and colorectal cancer, respectively. Each of these two VNTRs associated with a >2-fold range of risk across individuals. These results reveal a substantial and previously unappreciated role of non-coding VNTRs in human health and gene regulation.
    MeSH term(s) Humans ; Calcium Channels/genetics ; Colorectal Neoplasms/genetics ; Genome, Human ; Glaucoma/genetics ; Minisatellite Repeats ; Polymorphism, Genetic ; Eukaryotic Initiation Factor-3/genetics
    Chemical Substances Calcium Channels ; TMCO1 protein, human ; Eukaryotic Initiation Factor-3
    Language English
    Publishing date 2023-07-31
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 187009-9
    ISSN 1097-4172 ; 0092-8674
    ISSN (online) 1097-4172
    ISSN 0092-8674
    DOI 10.1016/j.cell.2023.07.002
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Protein-altering variants at copy number-variable regions influence diverse human phenotypes.

    Hujoel, Margaux L A / Handsaker, Robert E / Sherman, Maxwell A / Kamitaki, Nolan / Barton, Alison R / Mukamel, Ronen E / Terao, Chikashi / McCarroll, Steven A / Loh, Po-Ru

    Nature genetics

    2024  Volume 56, Issue 4, Page(s) 569–578

    Abstract: Copy number variants (CNVs) are among the largest genetic variants, yet CNVs have not been effectively ascertained in most genetic association studies. Here we ascertained protein-altering CNVs from UK Biobank whole-exome sequencing data (n = 468,570) ... ...

    Abstract Copy number variants (CNVs) are among the largest genetic variants, yet CNVs have not been effectively ascertained in most genetic association studies. Here we ascertained protein-altering CNVs from UK Biobank whole-exome sequencing data (n = 468,570) using haplotype-informed methods capable of detecting subexonic CNVs and variation within segmental duplications. Incorporating CNVs into analyses of rare variants predicted to cause gene loss of function (LOF) identified 100 associations of predicted LOF variants with 41 quantitative traits. A low-frequency partial deletion of RGL3 exon 6 conferred one of the strongest protective effects of gene LOF on hypertension risk (odds ratio = 0.86 (0.82-0.90)). Protein-coding variation in rapidly evolving gene families within segmental duplications-previously invisible to most analysis methods-generated some of the human genome's largest contributions to variation in type 2 diabetes risk, chronotype and blood cell traits. These results illustrate the potential for new genetic insights from genomic variation that has escaped large-scale analysis to date.
    MeSH term(s) Humans ; DNA Copy Number Variations/genetics ; Diabetes Mellitus, Type 2/genetics ; Phenotype ; Genetic Association Studies ; Exons
    Language English
    Publishing date 2024-03-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1108734-1
    ISSN 1546-1718 ; 1061-4036
    ISSN (online) 1546-1718
    ISSN 1061-4036
    DOI 10.1038/s41588-024-01684-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Sibling chimerism among microglia in marmosets.

    Del Rosario, Ricardo C H / Krienen, Fenna M / Zhang, Qiangge / Goldman, Melissa / Mello, Curtis / Lutservitz, Alyssa / Ichihara, Kiku / Wysoker, Alec / Nemesh, James / Feng, Guoping / McCarroll, Steven A

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Chimerism happens rarely among most mammals but is common in marmosets and tamarins, a result of fraternal twin or triplet birth patterns in ... ...

    Abstract Chimerism happens rarely among most mammals but is common in marmosets and tamarins, a result of fraternal twin or triplet birth patterns in which
    Language English
    Publishing date 2023-10-17
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.10.16.562516
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Hidden protein-altering variants influence diverse human phenotypes.

    Hujoel, Margaux L A / Handsaker, Robert E / Sherman, Maxwell A / Kamitaki, Nolan / Barton, Alison R / Mukamel, Ronen E / Terao, Chikashi / McCarroll, Steven A / Loh, Po-Ru

    bioRxiv : the preprint server for biology

    2023  

    Abstract: Structural variants (SVs) comprise the largest genetic variants, altering from 50 base pairs to megabases of DNA. However, SVs have not been effectively ascertained in most genetic association studies, leaving a key gap in our understanding of human ... ...

    Abstract Structural variants (SVs) comprise the largest genetic variants, altering from 50 base pairs to megabases of DNA. However, SVs have not been effectively ascertained in most genetic association studies, leaving a key gap in our understanding of human complex trait genetics. We ascertained protein-altering SVs from UK Biobank whole-exome sequencing data (
    Language English
    Publishing date 2023-06-09
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.06.07.544066
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Brain single cell transcriptomic profiles in episodic memory phenotypes associated with temporal lobe epilepsy.

    Busch, Robyn M / Yehia, Lamis / Hu, Bo / Goldman, Melissa / Hermann, Bruce P / Najm, Imad M / McCarroll, Steven A / Eng, Charis

    NPJ genomic medicine

    2022  Volume 7, Issue 1, Page(s) 69

    Abstract: Memory dysfunction is prevalent in temporal lobe epilepsy (TLE), but little is known about the underlying molecular etiologies. Single-nucleus RNA sequencing technology was used to examine differences in cellular heterogeneity among left (language- ... ...

    Abstract Memory dysfunction is prevalent in temporal lobe epilepsy (TLE), but little is known about the underlying molecular etiologies. Single-nucleus RNA sequencing technology was used to examine differences in cellular heterogeneity among left (language-dominant) temporal neocortical tissues from patients with TLE with (n = 4) or without (n = 2) impairment in verbal episodic memory. We observed marked cell heterogeneity between memory phenotypes and identified numerous differentially expressed genes across all brain cell types. The most notable differences were observed in glutamatergic (excitatory) and GABAergic (inhibitory) neurons with an overrepresentation of genes associated with long-term potentiation, long-term depression, and MAPK signaling, processes known to be essential for episodic memory formation.
    Language English
    Publishing date 2022-11-29
    Publishing country England
    Document type Journal Article
    ZDB-ID 2813848-X
    ISSN 2056-7944 ; 2056-7944
    ISSN (online) 2056-7944
    ISSN 2056-7944
    DOI 10.1038/s41525-022-00339-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Using Droplet Digital PCR to Analyze Allele-Specific RNA Expression.

    Kamitaki, Nolan / Usher, Christina L / McCarroll, Steven A

    Methods in molecular biology (Clifton, N.J.)

    2018  Volume 1768, Page(s) 401–422

    Abstract: Genome-wide association studies have discovered thousands of common alleles that associate with human phenotypes and disease. Many of these variants are in non-protein-coding (regulatory) regions and are believed to affect phenotypes by modifying gene ... ...

    Abstract Genome-wide association studies have discovered thousands of common alleles that associate with human phenotypes and disease. Many of these variants are in non-protein-coding (regulatory) regions and are believed to affect phenotypes by modifying gene expression. In any organism with a diploid genome, such as humans, measuring the expression of each allele of a gene provides a well-controlled way to identify allelic influences on that gene's expression. Here, we describe a protocol for precisely measuring the allele-specific expression of individual genes. This method targets the nucleotide differences between the two alleles of a gene within an individual and measures the "allelic skew," the extent to which one allele is expressed more than the other. We cover the design of effective assays, the optimization of reactions, and the interpretation of the resulting data.
    MeSH term(s) Alleles ; Allelic Imbalance/genetics ; Genetic Markers/genetics ; Humans ; Polymorphism, Single Nucleotide/genetics ; RNA/genetics ; RNA/isolation & purification ; Regulatory Sequences, Nucleic Acid/genetics ; Reverse Transcriptase Polymerase Chain Reaction/instrumentation ; Reverse Transcriptase Polymerase Chain Reaction/methods
    Chemical Substances Genetic Markers ; RNA (63231-63-0)
    Language English
    Publishing date 2018-04-30
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural
    ISSN 1940-6029
    ISSN (online) 1940-6029
    DOI 10.1007/978-1-4939-7778-9_23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Astrocytic cell adhesion genes linked to schizophrenia correlate with synaptic programs in neurons.

    Pietiläinen, Olli / Trehan, Aditi / Meyer, Daniel / Mitchell, Jana / Tegtmeyer, Matthew / Valakh, Vera / Gebre, Hilena / Chen, Theresa / Vartiainen, Emilia / Farhi, Samouil L / Eggan, Kevin / McCarroll, Steven A / Nehme, Ralda

    Cell reports

    2023  Volume 42, Issue 1, Page(s) 111988

    Abstract: The maturation of neurons and the development of synapses, although emblematic of neurons, also relies on interactions with astrocytes and other glia. Here, to study the role of glia-neuron interactions, we analyze the transcriptomes of human pluripotent ...

    Abstract The maturation of neurons and the development of synapses, although emblematic of neurons, also relies on interactions with astrocytes and other glia. Here, to study the role of glia-neuron interactions, we analyze the transcriptomes of human pluripotent stem cell (hPSC)-derived neurons, from 80 human donors, that were cultured with or without contact with glial cells. We find that the presence of astrocytes enhances synaptic gene-expression programs in neurons when in physical contact with astrocytes. These changes in neurons correlate with increased expression, in the cocultured glia, of genes that encode synaptic cell adhesion molecules. Both the neuronal and astrocyte gene-expression programs are enriched for genes associated with schizophrenia risk. Our results suggest that astrocyte-expressed genes with synaptic functions are associated with stronger expression of synaptic genetic programs in neurons, and they suggest a potential role for astrocyte-neuron interactions in schizophrenia.
    MeSH term(s) Humans ; Astrocytes/metabolism ; Cell Adhesion/genetics ; Schizophrenia/genetics ; Schizophrenia/metabolism ; Neurons/metabolism ; Neuroglia ; Synapses/physiology
    Language English
    Publishing date 2023-01-12
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2022.111988
    Database MEDical Literature Analysis and Retrieval System OnLINE

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