Genome in a Bottle Consortium-Progress and Planning Workshop, 226-227 [2015-33140]
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226
Federal Register / Vol. 81, No. 2 / Tuesday, January 5, 2016 / Notices
comparisons between competing
services. In the fall of 2015, the
California Division of Measurement
Standards submitted a proposal through
multiple regional weights and measures
associations to establish a separate NIST
Handbook 44 code to address
‘‘Transportation Network Services.’’ The
S&T Committee will examine these
proposals and the result of recent
discussions from a November 2015
USNWG meeting to assess how to best
address these systems.
L&R Committee
The following items are proposals to
amend NIST Handbook 130 or NIST
Handbook 133:
NIST Handbook 130—Section on
Uniform Regulation for the Method of
Sale of Commodities:
Item 232–7
Bedding
[FR Doc. 2015–33128 Filed 1–4–16; 8:45 am]
BILLING CODE 3510–13–P
DEPARTMENT OF COMMERCE
NIST Handbook 133—Chapter 3
Items 260–3 and 260–4 Section 3.14.
Firewood—(Volumetric Test Procedures
for Packaged Firewood with a Labeled
Volume of 113 L [4 ft3] or Less)
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Authority: 15 U.S.C. 272(b).
Richard Cavanagh,
Acting Associate Director for Laboratory
Programs.
Section 2.23. Animal
The L&R Committee will consider a
proposal to recommend adoption of a
uniform method of sale for animal
bedding that will enhance the ability of
consumers to make value comparisons
and will ensure fair competition.
Animal Bedding is generally defined as
any material, except for baled straw,
that is kept, offered or exposed for sale
or sold to retail consumers for primary
use as a medium for any pet or
companion or livestock animal to nest
or eliminate waste. If adopted, the
proposal will require packers to
advertise and sell packages of animal
bedding on the basis of the expanded
volume of the bedding. Most packages
of animal bedding are compressed
during packaging and the expanded
volume is the amount of product that
consumers will recover through
unwrapping and decompressing the
bedding according to the instructions
provided by the packer. See also Item
260–5, Section 3.15. Test Procedure for
Verifying the Usable Volume
Declaration on Packages of Animal
Bedding.
The current test procedure in NIST
Handbook 133, Section 3.14.,
Firewood—(Volumetric Test Procedure
for Packaged Firewood with a Labeled
Volume of 113 L [4 ft3] or Less) has
provided different test results when
applied in various state inspections. If
adopted, this proposal would clarify the
test procedure and improve the
accuracy of length determinations when
VerDate Sep<11>2014
determining the volume of wood in
bags, bundles and boxes. Improving the
test procedures will help ensure that
consumers can make value comparisons
and reduce unfair competition. Also
Item 232–4, NIST Handbook 130,
Method of Sale of Sale of Commodities
Regulation, Section 2.4. Fireplace and
Stove Wood, is being considered for
revision to recognize traditional
industry labeling practice and eliminate
language that appears to conflict with
the requirements of the Uniform
Packaging and Labeling Regulation.
18:43 Jan 04, 2016
Jkt 238001
National Institute of Standards and
Technology
Genome in a Bottle Consortium—
Progress and Planning Workshop
National Institute of Standards
and Technology, Commerce.
ACTION: Notice of public workshop.
AGENCY:
The National Institute of
Standards and Technology (NIST)
announces the Genome in a Bottle
Consortium—Progress and Planning
Workshop to be held on Thursday,
January 28, 2016, and Friday, January
29, 2016. The Genome in a Bottle
Consortium is developing the reference
materials, reference methods, and
reference data needed to assess
confidence in human whole genome
variant calls. A principal motivation for
this consortium is to enable
performance assessment of sequencing
and science-based regulatory oversight
of clinical sequencing. The purpose of
this workshop is to update participants
about progress of the consortium work,
continue to get broad input from
individual stakeholders to update or
refine the consortium work plan,
continue to broadly solicit consortium
membership from interested
stakeholders, and invite members to
participate in work plan
implementation.
Topics of discussion at this workshop
will include progress and planning of
the Analysis Group, which is analyzing
and integrating the large variety of
sequencing data for four candidate NIST
Reference Materials (RMs), with a
particular focus on challenging types of
variants and challenging regions of the
genome. Other potential NIST RMs that
SUMMARY:
PO 00000
Frm 00008
Fmt 4703
Sfmt 4703
might be developed by the consortium
will also be discussed.
DATES: The Genome in a Bottle
Consortium workshop will be held on
Thursday, January 28, 2016 from 9:00
a.m. to 5:30 p.m. Pacific Time, and
Friday, January 29, 2016 from 9:00 a.m.
to 1:00 p.m. Pacific Time. Attendees
must register by 5:00 p.m. Pacific Time
on Thursday, January 21, 2016.
ADDRESSES: The meeting will be held on
the second floor of the Li Ka Shing
Conference Center, Stanford University,
291 Campus Drive, Palo Alto, CA 94305.
Please note admittance instructions
under the SUPPLEMENTARY INFORMATION
section of this notice.
FOR FURTHER INFORMATION CONTACT: For
further information contact Justin Zook
by email at jzook@nist.gov or by phone
at (301) 975–4133 or Marc Salit by email
at salit@nist.gov or by phone at (650)
350–2338. To register, go to: https://
web.stanford.edu/∼saracl/GIAB2016.fb
SUPPLEMENTARY INFORMATION: Clinical
application of ultra high throughput
sequencing (UHTS) for hereditary
genetic diseases and oncology is rapidly
growing. At present, there are no widely
accepted genomic standards or
quantitative performance metrics for
confidence in variant calling. These
standards and quantitative performance
metrics are needed to achieve the
confidence in measurement results
expected for sound, reproducible
research and regulated applications in
the clinic. On April 13, 2012, NIST
convened the workshop ‘‘Genome in a
Bottle’’ to initiate a consortium to
develop the reference materials,
reference methods, and reference data
needed to assess confidence in human
whole genome variant calls
(www.genomeinabottle.org). On August
16–17, 2012, NIST hosted the first large
public meeting of the Genome in a
Bottle Consortium, with about 100
participants from government, academic
institutions, and industry. This meeting
was announced in the Federal Register
(77 FR 43237) on July 24, 2012. A
principal motivation for this consortium
was to enable science-based regulatory
oversight of clinical sequencing.
At the August 2012 meeting, the
consortium established work plans for
four technical working groups with the
following responsibilities:
(1) Reference Material (RM) Selection
and Design: Select appropriate sources
for whole genome RMs and identify or
design synthetic DNA constructs that
could be spiked-in to samples for
measurement assurance.
(2) Measurements for Reference
Material Characterization: Design and
carry out experiments to characterize
E:\FR\FM\05JAN1.SGM
05JAN1
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Federal Register / Vol. 81, No. 2 / Tuesday, January 5, 2016 / Notices
the RMs using multiple sequencing
methods, other methods, and validation
of selected variants using orthogonal
technologies.
(3) Bioinformatics, Data Integration,
and Data Representation: Develop
methods to analyze and integrate the
data for each RM, as well as select
appropriate formats to represent the
data.
(4) Performance Metrics and Figures
of Merit: Develop useful performance
metrics and figures of merit that can be
obtained through measurement of the
RMs.
The products of these technical
working groups will be a set of wellcharacterized whole genome and
synthetic DNA RMs along with the
methods (documentary standards) and
reference data necessary for use of the
RMs. These products will be designed to
help enable translation of whole genome
sequencing to regulated clinical
applications. The pilot, NIST ‘‘Human
DNA for Whole-Genome Variant
Assessment (Daughter of Utah/European
Ancestry)’’ RM was released in May
2015 and is available at https://
tinyurl.com/giabpilot. The consortium is
currently analyzing and integrating data
from two trios that are candidate NIST
RMs. The consortium meets in
workshops two times per year, in
January at Stanford University in Palo
Alto, CA, and in August at the National
Institute of Standards and Technology
in Gaithersburg, MD. At these
workshops, including the last meetings
at Stanford in January 2015 and at NIST
in August 2015, participants in the
consortium have discussed progress
developing well-characterized genomes
for NIST Reference Materials and
planned future experiments and
analysis of these genomes (see https://
federalregister.gov/a/2012-18064,
https://federalregister.gov/a/201318934, https://federalregister.gov/a/
2014-18841 and https://
federalregister.gov/a/2015-01158 for
past workshops at NIST and Stanford).
The January 2015 meeting was
announced in the Federal Register (80
FR 3220) on January 22, 2015, and the
meeting is summarized at https://
docs.google.com/document/d/19J6YDg
1MH1iD-8Q8mmV9L7wHOfuyUC3
aogctZ2Nh87U/edit?usp=sharing. The
August 2015 meeting was announced in
the Federal Register (80 FR 45194) on
July 29, 2015, and the meeting is
summarized at https://docs.google.com/
document/d/19-KSn0ydF8rsWRbl
6OqhIdbt2gGN10dOMRF6inKmrk4/
edit?usp=sharing.
There is no cost for participating in
the consortium. No proprietary
information will be shared as part of the
VerDate Sep<11>2014
18:43 Jan 04, 2016
Jkt 238001
consortium, and all research results will
be in the public domain.
All attendees are required to preregister. Anyone wishing to attend this
meeting must pre-register at https://
web.stanford.edu/∼saracl/GIAB2016.fb
by 5:00 p.m. Pacific Time on Thursday,
January 21, 2016, in order to attend.
Richard Cavanagh,
Acting Associate Director of Laboratory
Programs.
[FR Doc. 2015–33140 Filed 1–4–16; 8:45 am]
BILLING CODE 3510–13–P
DEPARTMENT OF COMMERCE
National Oceanic and Atmospheric
Administration
Proposed Information Collection;
Comment Request; Quantitative
Assessment of Spatially-Explicit Social
Values Relative to Wind Energy Areas:
Outer Continental Shelf Offshore North
Carolina
National Oceanic and
Atmospheric Administration (NOAA),
Commerce.
ACTION: Notice.
AGENCY:
The Department of
Commerce, as part of its continuing
effort to reduce paperwork and
respondent burden, invites the general
public and other Federal agencies to
take this opportunity to comment on
proposed and/or continuing information
collections, as required by the
Paperwork Reduction Act of 1995.
DATES: Written comments must be
submitted on or before March 7, 2016.
ADDRESSES: Direct all written comments
to Jennifer Jessup, Departmental
Paperwork Clearance Officer,
Department of Commerce, Room 6616,
14th and Constitution Avenue NW.,
Washington, DC 20230 (or via the
Internet at JJessup@doc.gov).
FOR FURTHER INFORMATION CONTACT:
Requests for additional information or
copies of the information collection
instrument and instructions should be
directed to Theresa L. Goedeke, 240–
533–0383 or theresa.goedeke@noaa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
I. Abstract
Pursuant to the Outer Continental
Shelf Land Act, the National
Environmental Policy Act and the
Coastal Zone Management Act, this
request is for a new data collection to
benefit the National Oceanic and
Atmospheric Administration (NOAA),
Bureau of Ocean Energy Management
(BOEM), and policy-makers on the state
PO 00000
Frm 00009
Fmt 4703
Sfmt 4703
227
and local level in North Carolina. BOEM
has identified three wind energy areas
for potential development on the outer
continental shelf of North Carolina. The
National Ocean Service (NOS) proposes
to collect data on the knowledge,
beliefs, social values, and attitudes of
North Carolina and South Carolina
residents relative to marine and coastal
landscapes, alternative energy
production options, and offshore wind
energy development. Respondents will
be sampled from households in eight to
ten coastal counties.
The required information will be used
to objectively assess the level of support
and/or opposition for offshore wind
energy development in the region, as
well as identify the relevant issues and
concerns most salient to residents. The
information will be used by BOEM,
NOAA, and others to improve agency
understanding about the beliefs, social
values, attitudes, and concerns of
people potentially affected by offshore
wind energy development. Such
information will be used to ascertain the
possible sociocultural outcomes of
offshore wind energy development in
the region, such as an enhancement or
reduction in enjoyment of the coastal
landscape/seascape. Additionally,
information collected will be used to
improve communication efforts targeted
to residents, enabling agencies to more
effectively and efficiently direct
outreach and community inclusion
activities.
II. Method of Collection
The data collection will take place
over a three to four month period and
will be comprised of a questionnaire to
be completed by the respondent. The
data will be collected via a mail-back
survey instrument.
III. Data
OMB Control Number: 0648–XXXX.
Form Number: None.
Type of Review: Regular submission
(request for a new information
collection).
Affected Public: Individuals or
households.
Estimated Number of Respondents:
4,000.
Estimated Time per Response: 20
minutes.
Estimated Total Annual Burden
Hours: 1,333.
Estimated Total Annual Cost to
Public: $0 in recordkeeping/reporting
costs.
IV. Request for Comments
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
E:\FR\FM\05JAN1.SGM
05JAN1
Agencies
[Federal Register Volume 81, Number 2 (Tuesday, January 5, 2016)]
[Notices]
[Pages 226-227]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-33140]
-----------------------------------------------------------------------
DEPARTMENT OF COMMERCE
National Institute of Standards and Technology
Genome in a Bottle Consortium--Progress and Planning Workshop
AGENCY: National Institute of Standards and Technology, Commerce.
ACTION: Notice of public workshop.
-----------------------------------------------------------------------
SUMMARY: The National Institute of Standards and Technology (NIST)
announces the Genome in a Bottle Consortium--Progress and Planning
Workshop to be held on Thursday, January 28, 2016, and Friday, January
29, 2016. The Genome in a Bottle Consortium is developing the reference
materials, reference methods, and reference data needed to assess
confidence in human whole genome variant calls. A principal motivation
for this consortium is to enable performance assessment of sequencing
and science-based regulatory oversight of clinical sequencing. The
purpose of this workshop is to update participants about progress of
the consortium work, continue to get broad input from individual
stakeholders to update or refine the consortium work plan, continue to
broadly solicit consortium membership from interested stakeholders, and
invite members to participate in work plan implementation.
Topics of discussion at this workshop will include progress and
planning of the Analysis Group, which is analyzing and integrating the
large variety of sequencing data for four candidate NIST Reference
Materials (RMs), with a particular focus on challenging types of
variants and challenging regions of the genome. Other potential NIST
RMs that might be developed by the consortium will also be discussed.
DATES: The Genome in a Bottle Consortium workshop will be held on
Thursday, January 28, 2016 from 9:00 a.m. to 5:30 p.m. Pacific Time,
and Friday, January 29, 2016 from 9:00 a.m. to 1:00 p.m. Pacific Time.
Attendees must register by 5:00 p.m. Pacific Time on Thursday, January
21, 2016.
ADDRESSES: The meeting will be held on the second floor of the Li Ka
Shing Conference Center, Stanford University, 291 Campus Drive, Palo
Alto, CA 94305. Please note admittance instructions under the
SUPPLEMENTARY INFORMATION section of this notice.
FOR FURTHER INFORMATION CONTACT: For further information contact Justin
Zook by email at jzook@nist.gov or by phone at (301) 975-4133 or Marc
Salit by email at salit@nist.gov or by phone at (650) 350-2338. To
register, go to: https://web.stanford.edu/~saracl/GIAB2016.fb
SUPPLEMENTARY INFORMATION: Clinical application of ultra high
throughput sequencing (UHTS) for hereditary genetic diseases and
oncology is rapidly growing. At present, there are no widely accepted
genomic standards or quantitative performance metrics for confidence in
variant calling. These standards and quantitative performance metrics
are needed to achieve the confidence in measurement results expected
for sound, reproducible research and regulated applications in the
clinic. On April 13, 2012, NIST convened the workshop ``Genome in a
Bottle'' to initiate a consortium to develop the reference materials,
reference methods, and reference data needed to assess confidence in
human whole genome variant calls (www.genomeinabottle.org). On August
16-17, 2012, NIST hosted the first large public meeting of the Genome
in a Bottle Consortium, with about 100 participants from government,
academic institutions, and industry. This meeting was announced in the
Federal Register (77 FR 43237) on July 24, 2012. A principal motivation
for this consortium was to enable science-based regulatory oversight of
clinical sequencing.
At the August 2012 meeting, the consortium established work plans
for four technical working groups with the following responsibilities:
(1) Reference Material (RM) Selection and Design: Select
appropriate sources for whole genome RMs and identify or design
synthetic DNA constructs that could be spiked-in to samples for
measurement assurance.
(2) Measurements for Reference Material Characterization: Design
and carry out experiments to characterize
[[Page 227]]
the RMs using multiple sequencing methods, other methods, and
validation of selected variants using orthogonal technologies.
(3) Bioinformatics, Data Integration, and Data Representation:
Develop methods to analyze and integrate the data for each RM, as well
as select appropriate formats to represent the data.
(4) Performance Metrics and Figures of Merit: Develop useful
performance metrics and figures of merit that can be obtained through
measurement of the RMs.
The products of these technical working groups will be a set of
well-characterized whole genome and synthetic DNA RMs along with the
methods (documentary standards) and reference data necessary for use of
the RMs. These products will be designed to help enable translation of
whole genome sequencing to regulated clinical applications. The pilot,
NIST ``Human DNA for Whole-Genome Variant Assessment (Daughter of Utah/
European Ancestry)'' RM was released in May 2015 and is available at
https://tinyurl.com/giabpilot. The consortium is currently analyzing and
integrating data from two trios that are candidate NIST RMs. The
consortium meets in workshops two times per year, in January at
Stanford University in Palo Alto, CA, and in August at the National
Institute of Standards and Technology in Gaithersburg, MD. At these
workshops, including the last meetings at Stanford in January 2015 and
at NIST in August 2015, participants in the consortium have discussed
progress developing well-characterized genomes for NIST Reference
Materials and planned future experiments and analysis of these genomes
(see https://federalregister.gov/a/2012-18064, https://federalregister.gov/a/2013-18934, https://federalregister.gov/a/2014-18841 and https://federalregister.gov/a/2015-01158 for past workshops
at NIST and Stanford). The January 2015 meeting was announced in the
Federal Register (80 FR 3220) on January 22, 2015, and the meeting is
summarized at https://docs.google.com/document/d/19J6YDg1MH1iD-8Q8mmV9L7wHOfuyUC3aogctZ2Nh87U/edit?usp=sharing. The August 2015
meeting was announced in the Federal Register (80 FR 45194) on July 29,
2015, and the meeting is summarized at https://docs.google.com/document/d/19-KSn0ydF8rsWRbl6OqhIdbt2gGN10dOMRF6inKmrk4/edit?usp=sharing.
There is no cost for participating in the consortium. No
proprietary information will be shared as part of the consortium, and
all research results will be in the public domain.
All attendees are required to pre-register. Anyone wishing to
attend this meeting must pre-register at https://web.stanford.edu/
~saracl/GIAB2016.fb by 5:00 p.m. Pacific Time on Thursday, January 21,
2016, in order to attend.
Richard Cavanagh,
Acting Associate Director of Laboratory Programs.
[FR Doc. 2015-33140 Filed 1-4-16; 8:45 am]
BILLING CODE 3510-13-P