Reference Signal Sequence Grouping for Inter-Cell Interference

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Solution Overview

Problem

The limited number of ZC sequences and the need to reuse sequences with the same sequence number in different cells leads to inter-cell interference and reduced accuracy in channel estimation due to limited transmission power and narrower bandwidths, especially in mobile communication systems.

Innovation Solution

Grouping R×M sequences specified by Zadoff-Chu sequence numbers and cyclic shift sequence numbers into sequence groups based on transmission bandwidths, and assigning these groups to cells to increase the number of available sequences and reduce interference.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If ZC sequences are reused in different cells to increase sequence availability, then the number of assignable sequences increases, but inter-cell interference increases and channel estimation accuracy deteriorates

Engineering Contradiction:
Improvenumber of assignable sequencesVSAvoidinter-cell interference
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The invention segments the limited ZC sequences into multiple groups (first group and second group). Cells are divided into different cell groups, with each cell group assigned sequences from a specific group. This segmentation allows sequence reuse across different cell groups while preventing interference within the same cell group, thereby increasing the number of assignable sequences without sacrificing channel estimation accuracy.

Inventive Principle:
Principle #1Segmentation

2Area of stationary object

If transmission bandwidth is reduced to extend coverage, then coverage area increases, but the number of available ZC sequences decreases

Engineering Contradiction:
Improvecoverage areaVSAvoidnumber of available ZC sequences
Core Design Contradiction:
Area of stationary objectVSQuantity of substance

Solution Approach 1:

By segmenting sequences into multiple groups and assigning different groups to different cell groups, the invention effectively multiplies the number of available sequences. This allows narrowband transmission (smaller bandwidth) to extend coverage area while maintaining sufficient sequence diversity through proper group assignment, preventing the degradation of sequence availability that would normally occur with reduced bandwidth.

Inventive Principle:
Principle #1Segmentation

3Reliability

If cyclic shift amount is increased to accommodate larger delay spread, then robustness to delay spread improves, but the number of usable cyclic shift sequences decreases

Engineering Contradiction:
Improverobustness to delay spreadVSAvoidnumber of usable cyclic shift sequences
Core Design Contradiction:
ReliabilityVSQuantity of substance

Solution Approach 1:

The invention segments sequences into multiple groups where each group can utilize a full set of cyclic shifts. By assigning different sequence groups to different cell groups, the system can afford to use larger cyclic shift amounts (reducing usable cyclic shifts per sequence) while still having sufficient total sequences available across all groups, thereby maintaining robustness to delay spread without sacrificing the number of usable sequences.

Inventive Principle:
Principle #1Segmentation

Data Source

PatentUS12556298B2Terminal apparatus and sequence assigning method
Publication Date: 2026.02.17 PANASONIC HOLDINGS CORP
  • US12556298B2 patent drawing
  • US12556298B2 patent drawing
  • US12556298B2 patent drawing

AI summary

Provided is a sequence allocation method capable of reducing inter-cell interference of a reference signal when a ZC sequence is used as the reference signal in a mobile communication system. In the sequence allocation method, R×M sequences specified by a ZC sequence number r (r=1 to R) and a cyclic shift sequence number m (m=1 to M) are divided into a plurality of sequence groups X (X=1 to R) in accordance with the transmission band width of the reference signal, so that the ZC sequence is allocated to each cell in each sequence group unit. When it is assumed that R=9 and M=6, the number of sequences is 54. Each of the sequence groups is formed by two sequences. Accordingly, the number of sequence groups is 27. The 27 types of sequence groups are allocated to each cell.