@deciphergenomics.bsky.social
Links to IEMbase and Treatable ID have moved – they can now be found on the new Therapies tab
January 28, 2026 at 12:49 PM
Links to IEMbase and Treatable ID have moved – they can now be found on the new Therapies tab
Approved genetic drugs/therapies, from the @n1collaborative.bsky.social, N1C Gene Registry are now displayed in DECIPHER on a new Therapies tab - available from gene pages and patient records.
January 28, 2026 at 12:48 PM
Approved genetic drugs/therapies, from the @n1collaborative.bsky.social, N1C Gene Registry are now displayed in DECIPHER on a new Therapies tab - available from gene pages and patient records.
Links to @uniquecharity.bsky.social single gene disorder guides are now displayed in DECIPHER on gene pages, therapies tabs and patient records #inclusion #informationforeveryone
January 28, 2026 at 12:47 PM
Links to @uniquecharity.bsky.social single gene disorder guides are now displayed in DECIPHER on gene pages, therapies tabs and patient records #inclusion #informationforeveryone
DECIPHER version 11.37 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
January 28, 2026 at 12:46 PM
DECIPHER version 11.37 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
I'm excited to be speaking at #FOGLondon this January.
Have a question you'd like me to answer during my session? Drop it in the comments or message me, I'd love to hear your thoughts.
Further information: hubs.la/Q03JMvwd0
#FOGLondon #genomics #biodata
Have a question you'd like me to answer during my session? Drop it in the comments or message me, I'd love to hear your thoughts.
Further information: hubs.la/Q03JMvwd0
#FOGLondon #genomics #biodata
December 3, 2025 at 10:17 AM
I'm excited to be speaking at #FOGLondon this January.
Have a question you'd like me to answer during my session? Drop it in the comments or message me, I'd love to hear your thoughts.
Further information: hubs.la/Q03JMvwd0
#FOGLondon #genomics #biodata
Have a question you'd like me to answer during my session? Drop it in the comments or message me, I'd love to hear your thoughts.
Further information: hubs.la/Q03JMvwd0
#FOGLondon #genomics #biodata
Reposted
Compiling evidence of gene-disease associations from the scientific literature for rare disease diagnosis and research is essential but time consuming.
Publications identified using a new machine learning approach can now be searched and browsed in G2P.
www.ebi.ac.uk/about/news/u...
Publications identified using a new machine learning approach can now be searched and browsed in G2P.
www.ebi.ac.uk/about/news/u...
Machine learning method identifies evidence for developmental disorders in the G2P database
An extensive collection of peer-reviewed publications describing developmental disorders has been identified and integrated into G2P to help clinicians and researchers better understand the genetic ba...
www.ebi.ac.uk
November 27, 2025 at 2:02 PM
Compiling evidence of gene-disease associations from the scientific literature for rare disease diagnosis and research is essential but time consuming.
Publications identified using a new machine learning approach can now be searched and browsed in G2P.
www.ebi.ac.uk/about/news/u...
Publications identified using a new machine learning approach can now be searched and browsed in G2P.
www.ebi.ac.uk/about/news/u...
On the protein browser mtDNA @gnomad-project.bsky.social missense and LoF tracks are available which display the location of gnomAD variants with these predicted molecular consequences.
October 31, 2025 at 10:09 AM
On the protein browser mtDNA @gnomad-project.bsky.social missense and LoF tracks are available which display the location of gnomAD variants with these predicted molecular consequences.
On the genome browser, @gnomad-project.bsky.social mitochondrial variants and coverage tracks are now available. Variants can be coloured by predicted consequence, homoplasmic allele frequency or heteroplasmic allele frequency.
October 31, 2025 at 10:08 AM
On the genome browser, @gnomad-project.bsky.social mitochondrial variants and coverage tracks are now available. Variants can be coloured by predicted consequence, homoplasmic allele frequency or heteroplasmic allele frequency.
On annotation tabs, @gnomad-project.bsky.social mitochondrial DNA variant homoplasmic and heteroplasmic counts and allele frequencies for each haplogroup are displayed alongside lineage information from MITOMAP. Heteroplasmy distribution and coverage metrics are also available
October 31, 2025 at 10:07 AM
On annotation tabs, @gnomad-project.bsky.social mitochondrial DNA variant homoplasmic and heteroplasmic counts and allele frequencies for each haplogroup are displayed alongside lineage information from MITOMAP. Heteroplasmy distribution and coverage metrics are also available
DECIPHER version 11.35 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
October 31, 2025 at 10:07 AM
DECIPHER version 11.35 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
Reposted
Growth charts guide child healthcare, but standard charts often don’t reflect the growth patterns of children with rare conditions.
A new method, LMSz, creates condition-specific growth charts and is being integrated in @deciphergenomics.bsky.social
www.ebi.ac.uk/about/news/t...
🧬💻
A new method, LMSz, creates condition-specific growth charts and is being integrated in @deciphergenomics.bsky.social
www.ebi.ac.uk/about/news/t...
🧬💻
New method to bring growth charts to children with rare genetic conditions through DECIPHER
A new method for building growth charts for children with rare diseases is being integrated into DECIPHER to help clinicians and families understand child development.
www.ebi.ac.uk
October 22, 2025 at 11:42 AM
Growth charts guide child healthcare, but standard charts often don’t reflect the growth patterns of children with rare conditions.
A new method, LMSz, creates condition-specific growth charts and is being integrated in @deciphergenomics.bsky.social
www.ebi.ac.uk/about/news/t...
🧬💻
A new method, LMSz, creates condition-specific growth charts and is being integrated in @deciphergenomics.bsky.social
www.ebi.ac.uk/about/news/t...
🧬💻
Reposted
Super-simple application of pathogenicity evidence during variant assessment in @deciphergenomics.bsky.social - even for complicated PVS1 in multiexon deletions where the frame is preserved - confirming a likely diagnosis.
September 11, 2025 at 8:25 AM
Super-simple application of pathogenicity evidence during variant assessment in @deciphergenomics.bsky.social - even for complicated PVS1 in multiexon deletions where the frame is preserved - confirming a likely diagnosis.
Reposted
Very cool new feature in @deciphergenomics.bsky.social - direct link from any missense variant to ProtVar @ebi.embl.org. This variant is in the binding site and likely interacts with the ligand, predicted using AlphaFold with AlphaFill!
September 10, 2025 at 9:54 AM
Very cool new feature in @deciphergenomics.bsky.social - direct link from any missense variant to ProtVar @ebi.embl.org. This variant is in the binding site and likely interacts with the ligand, predicted using AlphaFold with AlphaFill!
The bespoke PubMed search on gene pages is now displayed in bold. This link opens a browser tab with a PubMed search displaying publications that include the gene of interest.
September 10, 2025 at 3:50 PM
The bespoke PubMed search on gene pages is now displayed in bold. This link opens a browser tab with a PubMed search displaying publications that include the gene of interest.
Descriptive names for gene and protein predictive scores are now displayed on gene pages to assist in demystifying these scores and making them easier to understand.
September 10, 2025 at 3:50 PM
Descriptive names for gene and protein predictive scores are now displayed on gene pages to assist in demystifying these scores and making them easier to understand.
ClinGen Variant Curation Expert Panel Recommendations are now displayed more clearly on gene pages and in the pathogenicity evidence interface, especially for genes with recommendations for more than one disease @theacmg.bsky.social
September 10, 2025 at 3:49 PM
ClinGen Variant Curation Expert Panel Recommendations are now displayed more clearly on gene pages and in the pathogenicity evidence interface, especially for genes with recommendations for more than one disease @theacmg.bsky.social
Links to ProtVar are now available from the protein browser which provide functional and structural annotations for missense variants @ebi.embl.org
September 10, 2025 at 3:49 PM
Links to ProtVar are now available from the protein browser which provide functional and structural annotations for missense variants @ebi.embl.org
Mitochondrial gene predictive scores are now displayed on gene pages which indicate the observed depletion or enrichment of specific variants classes in @gnomad-project.bsky.social l compared to a mitochondrial genome constraint model under neutrality selection.
September 10, 2025 at 3:48 PM
Mitochondrial gene predictive scores are now displayed on gene pages which indicate the observed depletion or enrichment of specific variants classes in @gnomad-project.bsky.social l compared to a mitochondrial genome constraint model under neutrality selection.
DECIPHER version 11.34 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
September 10, 2025 at 3:47 PM
DECIPHER version 11.34 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
Reposted
FASTKD5-related Leigh syndrome added to DDG2P. Biallelic FASTKD5 LoF variants cause an early- to late-onset Leigh syndrome associated with complex IV deficiency. www.ebi.ac.uk/gene2phenoty...
July 17, 2025 at 9:55 AM
FASTKD5-related Leigh syndrome added to DDG2P. Biallelic FASTKD5 LoF variants cause an early- to late-onset Leigh syndrome associated with complex IV deficiency. www.ebi.ac.uk/gene2phenoty...
Reposted
'UGGT1-related congenital disorder of glycosylation with neurodevelopmental impairment' added to DDG2P. Biallelic UGGT1 LoF variants cause a disorder characterised by developmental delay, intellectual disability, seizures, craniofacial dysmorphism, and microcephaly. See www.ebi.ac.uk/gene2phenoty...
July 11, 2025 at 9:20 AM
'UGGT1-related congenital disorder of glycosylation with neurodevelopmental impairment' added to DDG2P. Biallelic UGGT1 LoF variants cause a disorder characterised by developmental delay, intellectual disability, seizures, craniofacial dysmorphism, and microcephaly. See www.ebi.ac.uk/gene2phenoty...
18 additional @gnomad-project.bsky.social short tandem repeats are now displayed; 9 recently discovered and 9 which are not currently linked to rare diseases but have historically appeared in various catalogs as suspected disease-causing loci.
July 10, 2025 at 9:07 AM
18 additional @gnomad-project.bsky.social short tandem repeats are now displayed; 9 recently discovered and 9 which are not currently linked to rare diseases but have historically appeared in various catalogs as suspected disease-causing loci.
Additional functional data from Multiplexed Assays of Variant Effect (MAVEs) are now displayed on functional tabs. Previously only published datasets were displayed, now datasets with a preprint are available @varianteffect.bsky.social
July 10, 2025 at 9:06 AM
Additional functional data from Multiplexed Assays of Variant Effect (MAVEs) are now displayed on functional tabs. Previously only published datasets were displayed, now datasets with a preprint are available @varianteffect.bsky.social
DECIPHER version 11.33 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
July 10, 2025 at 9:05 AM
DECIPHER version 11.33 has been released. See the new features at www.deciphergenomics.org #variantinterpretation
Reposted
Unravel the complexities of genome variation with our FREE online course! #FLGenomicVariantsDiversity
🗓️ Starts: 7 July
Learn how to get the most from #genomics data from diverse populations, using variant classification and interpretation approaches. #GenomeVariation🧬
📎bit.ly/3R7G7aK
🗓️ Starts: 7 July
Learn how to get the most from #genomics data from diverse populations, using variant classification and interpretation approaches. #GenomeVariation🧬
📎bit.ly/3R7G7aK
July 3, 2025 at 9:00 AM
Unravel the complexities of genome variation with our FREE online course! #FLGenomicVariantsDiversity
🗓️ Starts: 7 July
Learn how to get the most from #genomics data from diverse populations, using variant classification and interpretation approaches. #GenomeVariation🧬
📎bit.ly/3R7G7aK
🗓️ Starts: 7 July
Learn how to get the most from #genomics data from diverse populations, using variant classification and interpretation approaches. #GenomeVariation🧬
📎bit.ly/3R7G7aK