BankIt Submitters: GenBank Submission Update

BankIt Submitters: GenBank Submission Update

As previously announced, major changes are being made to enhance your GenBank submission experience. As of April 2026, you can submit to GenBank using our new simplified wizards in Submission Portal-GenBank. 

What now? 
  • Use Submission Portal-GenBank for all GenBank sequence submissions, except for sequence alignments 
  • Use BankIt only if you are submitting aligned sequences for feature propagation 

Continue reading “BankIt Submitters: GenBank Submission Update”

Now Available: RefSeq Release 235

Now Available: RefSeq Release 235

RefSeq release 235 is now available online and from the FTP site! You can access RefSeq data through NCBI Datasets. The release is provided in several directories as a complete dataset and also as divided by logical groupings.    

What’s included in this release? 

As of May 11, 2026, this full release incorporates genomic, transcript, and protein data containing:   

  • 616,942,961 records  
  • 473,570,633 proteins  
  • 81,124,747 RNAs  
  • Sequences from 180,620 organisms  

Continue reading “Now Available: RefSeq Release 235”

New Data Available! Access Hantavirus Sequences at NCBI

New Data Available! Access Hantavirus Sequences at NCBI

Sequence data from the recent Andes hantavirus outbreak are now available through NLM’s NCBI resources, NCBI Virus web interface and NCBI Datasets command-line tool. These data were submitted by the University Hospitals of Geneva. 

Access through NCBI Virus 

To find sequence records from 2026, search for “Orthohantavirus andesense” in NCBI Virus and apply the “Collection Date” filter. To get a quick overview of Andes hantavirus data available through GenBank, visit the NCBI Virus Outbreak Statistics page (select Andes hantavirus) which shows the collection location and host for recently collected samples.   Continue reading “New Data Available! Access Hantavirus Sequences at NCBI”

Protocol Registration and Results System (PRS) Modernization

Protocol Registration and Results System (PRS) Modernization

Phasing out the Classic PRS 

The National Library of Medicine (NLM) has completed modernization of the Protocol Registration and Results System (PRS) and the public website, ClinicalTrials.gov. The Modernized PRS is now the primary system for protocol registration and results submission, and we will continue to add new features based on your feedback!  

Modernized PRS updates and new features 

Highlights of updated and upcoming features:  Continue reading “Protocol Registration and Results System (PRS) Modernization”

New: May 2026 Release of Stand-Alone PGAP

New: May 2026 Release of Stand-Alone PGAP

With New Evidence Source for Protein Naming 

We are happy to announce the release of a new version of the stand-alone Prokaryotic Genome Annotation Pipeline (PGAP)! 

What’s new? 
  • Software updated to CheckM 1.2.5 
  • Ongoing improved protein family model data used for annotation 
  • Pfam release 38 is being used for structural and functional annotation 
  • New evidence source: superfamilies 

As with previous releases, curators at NCBI continue to expand the library of Protein Family Models (PFMs) used by PGAP for structural and functional annotation.  Continue reading “New: May 2026 Release of Stand-Alone PGAP”

Updates to the NIH Manuscript Submission (NIHMS) System

Updates to the NIH Manuscript Submission (NIHMS) System

In Support of the 2024 NIH Public Access Policy

As part of continued enhancements to offerings to support NIH-funded researchers and institutions with compliance with the 2024 NIH Public Access Policy, the National Center for Biotechnology Information (NCBI) at the National Library of Medicine (NLM) recently updated the NIH Manuscript Submission (NIHMS) system to facilitate review of submitted Author Accepted Manuscripts.  

What has been updated?  

The NIHMS submission interface (see Figure 1) has been updated to assist Reviewers in applying the correct embargo as outlined in the 2024 NIH Public Access Policy. To learn more about the NIHMS process, see the Help documentation and NIHMS FAQs.  Continue reading “Updates to the NIH Manuscript Submission (NIHMS) System”

Reminder! NCBI is Retiring rsync for FTP Downloads June 1, 2026

Announcing brownout periods when rsync will be disabled 

As we previously announced, NCBI will discontinue support for the rsync protocol on June 1, 2026, as part of our ongoing effort to enhance security and efficiency. After June 1, attempts to connect to ftp.ncbi.nlm.gov using rsync will fail. To support this transition, we are announcing two temporary “brownout” periods. During these planned intervals, rsync access will be intentionally disabled to help our users identify and update affected workflows.   

Brownout schedule 

Rsync will be disabled during the following periods (all times are EDT): 

  • Tuesday, May 12, 2026, from 9 AM until 3 PM
  • Wednesday, May 27, 2026, from 9 AM until 3 PM 

Continue reading “Reminder! NCBI is Retiring rsync for FTP Downloads June 1, 2026”

GenBank Release 271.0 is Available!

GenBank Release 271.0 is Available!

GenBank release 271.0 (4/14/2026) is now available on the NCBI FTP site. This release has 53.90 trillion bases and 6.27 billion records. 

The current release has:  

  • 261,460,182 traditional records containing 7,289,942,983,522 base pairs of sequence data
  • 4,756,526,485 WGS records containing 45,628,511,953,497 base pairs of sequence data
  • 1,058,643,373 bulk-oriented TSA records containing 898,651,493,967 base pairs of sequence data
  • 191,365,090 bulk-oriented TLS records containing 79,162,820,303 base pairs of sequence data

Continue reading “GenBank Release 271.0 is Available!”

ClinVar’s New Search Interface and Homepage are Here!

ClinVar’s New Search Interface and Homepage are Here!

ClinVar is a free, public resource you can use to research the clinical significance of genetic variants. Many people visit ClinVar multiple times a day! We previously announced an upcoming enhanced search experience and new ClinVar homepage, and these improvements are now live. 

What’s new?  

Search enhancements 

The new search interface provides different search boxes for the types of terms typically used to search ClinVar. These search boxes provide additional help with syntax. One or more terms can be combined to create more complex searches. A “more search options” section can also be expanded to enter more atypical terms.   Continue reading “ClinVar’s New Search Interface and Homepage are Here!”

PMC Continues to Improve New Search

PMC Continues to Improve New Search

In September 2025, PubMed Central (PMC) launched a new full text search. Some previously available features were not included in the initial release. Now, PMC is rolling out additional search features based on your feedback. 

What’s new? 

Page navigation  

PMC recently updated the search results interface to make it easier to navigate your results and customize how they appear. 

Page navigation now appears at both the top and bottom of the results page, with one-click options to jump to the first, previous, next, or last page. You can enter a number to jump to a specific page of results. If you prefer to scroll through a single, expanding list, you can still select “Show More Results.”  Continue reading “PMC Continues to Improve New Search”