1. GenBank: The Nucleotide Sequence Database
pZ|{p{_j Ilene Mizrachi
) dk|S\ Created: October 9, 2002
2_HIn Updated: August 22, 2007
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i Summary
63l&
ihj The GenBank sequence database is an annotated collection of all publicly available nucleotide
3f^Pr sequences and their protein translations. This database is produced at National Center for
)S+fc= Biotechnology Information (NCBI) as part of an international collaboration with the European Molecular
Y|r7gy9% Biology Laboratory (EMBL) Data Library from the European Bioinformatics Institute (EBI) and the DNA
*
rlVE Data Bank of Japan (DDBJ). GenBank and its collaborators receive sequences produced in
4xg)e`
*U laboratories throughout the world from more than 100,000 distinct organisms. GenBank continues to
pTq DPU grow at an exponential rate, doubling every 10 months. Release 134, produced in February 2003,
^4
$4x contained over 29.3 billion nucleotide bases in more than 23.0 million sequences. GenBank is built
1xS+r)_n@ by direct submissions from individual laboratories, as well as from bulk submissions from large-scale
;:
_K,FU sequencing centers.
i#b /.oa Direct submissions are made to GenBank using BankIt [
http://www.ncbi.nlm.nih.gov/BankIt/],
k/{WlLN which is a Web-based form, or the stand-alone submission program, Sequin [http://
uT,i& www.ncbi.nlm.nih.gov/Sequin/index.html]. Upon receipt of a sequence submission, the GenBank staff
~;CNWJtcf( assigns an Accession number to the sequence and performs quality assurance checks. The
uc+{<E3,% submissions are then released to the public database, where the entries are retrievable by Entrez or
>R]M:Wx downloadable by FTP. Bulk submissions of Expressed Sequence Tag (EST), Sequence Tagged Site
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C [O (STS), Genome Survey Sequence (GSS), and High-Throughput Genome Sequence (HTGS) data are
,==_u most often submitted by large-scale sequencing centers. The GenBank direct submissions group also
!0?o3,of- processes complete microbial genome sequences.
fdKE1,; History
EP@u4F Initially, GenBank was built and maintained at Los Alamos National Laboratory (LANL). In the early
JS ^Cc 1990s, this responsibility was awarded to NCBI through congressional mandate. NCBI undertook
%z@ Z^Jv the task of scanning the literature for sequences and manually typing the sequences into the data-
}_KzF~ base. Staff then added annotation to these records, based upon information in the published article.
Lp:VU-S Scanning sequences from the literature and placing them into GenBank is now a rare occurrence.
#[9UCX^= Nearly all of the sequences are now deposited directly by the labs that generate the sequences.
_1E c54D This is attributable to, in part, a requirement by most journal publishers that nucleotide sequences
X,VI5$ are first deposited into publicly available databases (DDBJ/EMBL/GenBank) so that the Accession
8%B_nVc number can be cited and the sequence can be retrieved when the article is published. NCBI began
0,RYO :`
1-1
r2\%/9uO h +B7BjA>G NCBI Handbook GenBank
<J+Oh\8tad accepting direct submissions to GenBank in 1993 and received data from LANL until 1996. Cur-
vVo'f|fW rently, NCBI receives and processes about 20,000 direct submission sequences per month, in
^AU-hVj addition to the approximately 200,000 bulk submissions that are processed automatically.
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MxShUU International Collaboration
:'Gn?dv| In the mid-1990s, the GenBank database became part of the International Nucleotide Sequence
05ClPT\BCr Database Collaboration with the EMBL database (European Bioinformatics Institute [http://
#3
E"Ame www.ebi.ac.uk/], Hinxton, United Kingdom) and the Genome Sequence Database (GSDB; LANL,
]2f-oz*hU Los Alamos, NM). Subsequently, the GSDB was removed from the Collaboration (by the National
n+sv2Wv: Center for Genome Resources, Santa Fe, NM), and DDBJ [
http://www.ddbj.nig.ac.jp/] (Mishima,
3LfF{ED@ Japan) joined the group. Each database has its own set of submission and retrieval tools, but the
wp1O*)/q three databases exchange data daily so that all three databases should contain the same set of
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sequences. Members of the DDBJ, EMBL, and GenBank staff meet annually to discuss technical
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F1e:( issues, and an international advisory board meets with the database staff to provide additional
wT!?.Y)aj guidance. An entry can only be updated by the database that initially prepared it to avoid conflicting
^}$t(t data at the three sites.
bgE]Wk0 The Collaboration created a Feature Table Definition [
http://www.ncbi.nlm.nih.gov/collab/FT/ 0(+<uo~6p1 index.html] that outlines legal features and syntax for the DDBJ, EMBL, and GenBank feature tables.
i5le0lM The purpose of this document is to standardize annotation across the databases. The presentation
=Ks&m4 and format of the data are different in the three databases, however, the underlying biological infor-
Ue Ci{W mation is the same.
WDx
cV% Confidentiality of Data
[x7Rq_^ When scientists submit data to GenBank, they have the opportunity to keep their data confidential
'Y2$9qy-L for a specified period of time. This helps to allay concerns that the availability of their data in Gen-
KtAEM;g Bank before publication may compromise their work. When the article containing the citation of the
E7h@Y~bNhW sequence or its Accession number is published, the sequence record is released. The database
?&:N|cltD staff request that submitters notify GenBank of the date of publication so that the sequence can be
X_X7fRC0 released without delay. The request to release should be sent to
gb-admin@ncbi.nlm.nih.gov.
prS%lg>
Direct Submissions
?84f\<" The typical GenBank submission consists of a single, contiguous stretch of DNA or RNA sequence
]vcT2lr] with annotations. The annotations are meant to provide an adequate representation of the biological
^3sv2wh^|8 information in the record. The GenBank Feature Table Definition [
http://www.ncbi.nlm.nih.gov/col- Ma?uB8o+~ lab/FT/index.html] describes the various features and subsequent qualifiers agreed upon by the
W!ug^2" International Nucleotide Sequence Database Collaboration.
hO> q|+mC Currently, only nucleotide sequences are accepted for direct submission to GenBank. These
]v:,<=S include mRNA sequences with coding regions, fragments of genomic DNA with a single gene or
'g<{l&u multiple genes, and ribosomal RNA gene clusters. If part of the nucleotide sequence encodes a
.6[8$8c 1-2
nl2Lqu1 #"A`:bjG NCBI Handbook GenBank
.mrv"k\< protein, a conceptual translation, called a CDS (coding sequence), is annotated. The span of the
P2ySjgd CDS feature is mapped to the nucleotide sequence encoding the protein. A protein Accession num-
]2"UR_x ber (/protein_id) is assigned to the translation product, which will subsequently be added to the
B_Gcz5 protein databases.
S
e[=$W Multiple sequences can be submitted together. Such batch submissions of non-related sequen-
D`41\#ti ces may be processed together but will be displayed in Entrez (Chapter 15) as single records.
!4^Lv{1QZ Alternatively, by using the Sequin submission tool (Chapter 12), a submitter can specify that several
ql.[Uq sequences are biologically related. Such sequences are classified as environmental sample sets,
8}[<3K%*g population sets, phylogenetic sets, mutation sets, or segmented sets. Each sequence within a set
ok ,O/|E}? is assigned its own Accession number and can be viewed independently in Entrez. However, with
gmTBp}3 the exception of segmented sets, each set is also indexed within the PopSet division of Entrez, thus
~,F]~|U7l allowing scientists to view the relationship between the sequences.
gYho$E What defines a set? Environmental sample, population, phylogenetic, and mutation sets all
C4X3;l Z%S contain a group of sequences that spans the same gene or region of the genome. Environmental
Z1W
%fT samples are derived from a group of unclassified or unknown organisms. A population set contains
dXn$XGF%R sequences from different isolates of the same organism. A phylogenetic set contains sequences
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Dm from different organisms that are used to determine the phylogenetic relationship between them.
nmL|v Sequencing multiple mutations within a single gene gives rise to a mutation set.
?gU-a All sets, except segmented sets, may contain an alignment of the sequences within them and
#.]W>h
N8\ might include external sequences already present in the database. In fact, the submitter can begin
Vd.XZ*}r* with an existing alignment to create a submission to the database using the Sequin submission tool.
GdScYAC
Currently, Sequin accepts FASTA+GAP, PHYLIP, MACAW, NEXUS Interleaved, and NEXUS Con-
7]5+%[Dg! tiguous alignments. Submitted alignments will be displayed in the PopSet section of Entrez.
!:vQg+S Segmented sets are a collection of noncontiguous sequences that cover a specified genetic
4u2_xbT region. The most common example is a set of genomic sequences containing exons from a single
e=jtF"& gene where part or all of the intervening regions have not been sequenced. Each member record
FbdC3G|oA within the set contains the appropriate annotation, exon features in this case. However, the mRNA
?<0'h{z Ny and CDS will be annotated as joined features across the individual records. Segmented sets them-
~h +B&F+5 selves can be part of an environmental sample, population, phylogenetic, or mutation set.